HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423756_23423757delinsCA , CM000676.2:g.23423756_23423757delinsCA | GRCh38 |
NC_000014.8:g.23892965_23892966delinsCA , CM000676.1:g.23892965_23892966delinsCA | GRCh37 |
NC_000014.7:g.22962805_22962806delinsCA | NCBI36 |
NG_007884.1:g.16905_16906delinsTG , LRG_384:g.16905_16906delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2923-34_2923-33delinsTG MANE Select | ENSP00000347507.3:n.2923-34_2923-33delinsTG | |
ENST00000355349.3:c.2923-34_2923-33delinsTG | ENSP00000347507.3:n.2923-34_2923-33delinsTG | |
NM_000257.3:c.2923-34_2923-33delinsTG | NP_000248.2:n.2923-34_2923-33delinsTG | |
XR_245686.3:n.3029-34_3029-33delinsTG | ||
XM_017021340.1:c.2923-34_2923-33delinsTG | XP_016876829.1:n.2923-34_2923-33delinsTG | |
NM_000257.4:c.2923-34_2923-33delinsTG MANE Select | NP_000248.2:n.2923-34_2923-33delinsTG |