HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12810769A>C , CM000686.2:g.12810769A>C | GRCh38 |
NC_000024.9:g.14922704A>C , CM000686.1:g.14922704A>C | GRCh37 |
NC_000024.8:g.13432098A>C | NCBI36 |
NG_008311.1:g.114545A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651177.1:c.4190A>C | ENSP00000498372.1:p.Asn1397Thr | |
ENST00000338981.7:c.4190A>C MANE Select | ENSP00000342812.3:p.Asn1397Thr | |
ENST00000426564.6:n.4202A>C | ||
NM_004654.3:c.4190A>C | NP_004645.2:p.Asn1397Thr | |
XM_011531469.1:c.4190A>C | XP_011529771.1:p.Asn1397Thr | |
XM_011531470.1:c.3956A>C | XP_011529772.1:p.Asn1319Thr | |
XM_017030078.2:c.4205A>C | XP_016885567.1:p.Asn1402Thr | |
NM_004654.4:c.4190A>C MANE Select | NP_004645.2:p.Asn1397Thr |