HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764617A>G , CM000674.2:g.57764617A>G | GRCh38 |
NC_000012.11:g.58158400A>G , CM000674.1:g.58158400A>G | GRCh37 |
NC_000012.10:g.56444667A>G | NCBI36 |
NG_007076.1:g.7577T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000713544.1:c.1045-67T>C | ENSP00000518840.1:n.1045-67T>C | |
ENST00000713545.1:c.1022-67T>C | ENSP00000518841.1:n.1022-67T>C | |
ENST00000228606.9:c.964-67T>C MANE Select | ENSP00000228606.4:n.964-67T>C | |
ENST00000228606.8:c.964-67T>C | ENSP00000228606.4:n.964-67T>C | |
ENST00000546567.5:c.259-67T>C | ENSP00000449472.1:n.259-67T>C | |
ENST00000547344.5:n.1103-67T>C | ||
ENST00000547451.1:n.900T>C | ||
NM_000785.3:c.964-67T>C | NP_000776.1:n.964-67T>C | |
NM_000785.4:c.964-67T>C MANE Select | NP_000776.1:n.964-67T>C |