HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75005809C>T , CM000676.2:g.75005809C>T | GRCh38 |
NC_000014.8:g.75472512C>T , CM000676.1:g.75472512C>T | GRCh37 |
NC_000014.7:g.74542265C>T | NCBI36 |
NG_013333.1:g.7901C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266126.10:c.598-57C>T MANE Select | ENSP00000266126.5:n.598-57C>T | |
ENST00000266126.9:c.598-57C>T | ENSP00000266126.5:n.598-57C>T | |
ENST00000553401.5:c.571-32C>T | ENSP00000451681.1:n.571-32C>T | |
ENST00000556028.5:c.598-88C>T | ENSP00000452311.1:n.598-88C>T | |
NM_014239.3:c.598-57C>T | NP_055054.1:n.598-57C>T | |
NM_014239.4:c.598-57C>T MANE Select | NP_055054.1:n.598-57C>T |