HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57763622C>T , CM000674.2:g.57763622C>T | GRCh38 |
NC_000012.11:g.58157405C>T , CM000674.1:g.58157405C>T | GRCh37 |
NC_000012.10:g.56443672C>T | NCBI36 |
NG_007076.1:g.8572G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000713544.1:c.1483G>A | ENSP00000518840.1:p.Ala495Thr | |
ENST00000713545.1:c.*407G>A | ENSP00000518841.1:n.*407G>A | |
ENST00000228606.9:c.1402G>A MANE Select | ENSP00000228606.4:p.Ala468Thr | |
ENST00000228606.8:c.1402G>A | ENSP00000228606.4:p.Ala468Thr | |
ENST00000547344.5:n.1541G>A | ||
NM_000785.3:c.1402G>A | NP_000776.1:p.Ala468Thr | |
NM_000785.4:c.1402G>A MANE Select | NP_000776.1:p.Ala468Thr |