HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816384G>T , CM000681.2:g.4816384G>T | GRCh38 |
NC_000019.9:g.4816396G>T , CM000681.1:g.4816396G>T | GRCh37 |
NC_000019.8:g.4767396G>T | NCBI36 |
NG_031998.1:g.20359C>A , LRG_358:g.20359C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.1994C>A MANE Select | ENSP00000248244.4:p.Thr665Lys | |
ENST00000248244.5:c.1994C>A | ENSP00000248244.4:p.Thr665Lys | |
ENST00000621756.1:c.1496C>A | ENSP00000479467.1:p.Thr499Lys | |
NM_182919.3:c.1994C>A , LRG_358t1:c.1994C>A | NP_891549.1:p.Thr665Lys | |
NM_001385678.1:c.1952C>A | NP_001372607.1:p.Thr651Lys | |
NM_001385679.1:c.1859C>A | NP_001372608.1:p.Thr620Lys | |
NM_001385680.1:c.1352C>A | NP_001372609.1:p.Thr451Lys | |
NM_182919.4:c.1994C>A MANE Select | NP_891549.1:p.Thr665Lys |