HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107710156A>C , CM000669.2:g.107710156A>C | GRCh38 |
NC_000007.13:g.107350601A>C , CM000669.1:g.107350601A>C | GRCh37 |
NC_000007.12:g.107137837A>C | NCBI36 |
NG_008489.1:g.54522A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.2192A>C MANE Select | ENSP00000494017.1:p.Asn731Thr | |
ENST00000644846.1:c.848A>C | ||
ENST00000265715.7:c.2192A>C | ENSP00000265715.3:p.Asn731Thr | |
ENST00000492030.2:n.378A>C | ||
NM_000441.1:c.2192A>C | NP_000432.1:p.Asn731Thr | |
XM_005250425.1:c.2192A>C | XP_005250482.1:p.Asn731Thr | |
XM_005250425.2:c.2192A>C | XP_005250482.1:p.Asn731Thr | |
XM_017012318.1:c.2114A>C | XP_016867807.1:p.Asn705Thr | |
NM_000441.2:c.2192A>C MANE Select | NP_000432.1:p.Asn731Thr |