HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23417324_23417325delinsCG , CM000676.2:g.23417324_23417325delinsCG | GRCh38 |
NC_000014.8:g.23886533_23886534delinsCG , CM000676.1:g.23886533_23886534delinsCG | GRCh37 |
NC_000014.7:g.22956373_22956374delinsCG | NCBI36 |
NG_007884.1:g.23337_23338delinsCG , LRG_384:g.23337_23338delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.4354-7_4354-6delinsCG (MYH7) MANE Select | ENSP00000347507.3:n.4354-7_4354-6delinsCG | |
ENST00000355349.3:c.4354-7_4354-6delinsCG (MYH7) | ENSP00000347507.3:n.4354-7_4354-6delinsCG | |
NM_000257.3:c.4354-7_4354-6delinsCG (MYH7) | NP_000248.2:n.4354-7_4354-6delinsCG | |
NR_126491.1:n.764_765delinsCG (MHRT) | ||
XM_017021340.1:c.4354-7_4354-6delinsCG (MYH7) | XP_016876829.1:n.4354-7_4354-6delinsCG | |
NM_000257.4:c.4354-7_4354-6delinsCG (MYH7) MANE Select | NP_000248.2:n.4354-7_4354-6delinsCG |