HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15879150G>A , CM000681.2:g.15879150G>A | GRCh38 |
NC_000019.9:g.15989960G>A , CM000681.1:g.15989960G>A | GRCh37 |
NC_000019.8:g.15850960G>A | NCBI36 |
NG_007971.2:g.23925C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221700.11:c.1397+196C>T MANE Select | ENSP00000221700.3:n.1397+196C>T | |
ENST00000011989.11:c.1397+196C>T | ENSP00000011989.8:n.1397+196C>T | |
ENST00000221700.10:c.1397+196C>T | ENSP00000221700.3:n.1397+196C>T | |
ENST00000392846.7:n.1340+196C>T | ||
ENST00000589654.2:c.185+196C>T | ||
NM_001082.4:c.1397+196C>T | NP_001073.3:n.1397+196C>T | |
NM_001082.5:c.1397+196C>T MANE Select | NP_001073.3:n.1397+196C>T |