HGVS | Genome Assembly |
---|---|
NC_000009.12:g.130872214G>T , CM000671.2:g.130872214G>T | GRCh38 |
NC_000009.11:g.133747601G>T , CM000671.1:g.133747601G>T | GRCh37 |
NC_000009.10:g.132737422G>T | NCBI36 |
NG_012034.1:g.163334G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372348.9:c.964+1G>T | ENSP00000361423.2:n.964+1G>T | |
ENST00000318560.6:c.907+1G>T MANE Select | ENSP00000323315.5:n.907+1G>T | |
ENST00000372348.7:c.964+1G>T | ENSP00000361423.2:n.964+1G>T | |
ENST00000318560.5:c.907+1G>T | ENSP00000323315.5:n.907+1G>T | |
ENST00000372348.6:c.964+1G>T | ENSP00000361423.2:n.964+1G>T | |
NM_005157.5:c.907+1G>T | NP_005148.2:n.907+1G>T | |
NM_007313.2:c.964+1G>T | NP_009297.2:n.964+1G>T | |
NM_005157.6:c.907+1G>T MANE Select | NP_005148.2:n.907+1G>T | |
NM_007313.3:c.964+1G>T | NP_009297.2:n.964+1G>T |