HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55096611C>T , CM000666.2:g.55096611C>T | GRCh38 |
NC_000004.11:g.55962778C>T , CM000666.1:g.55962778C>T | GRCh37 |
NC_000004.10:g.55657535C>T | NCBI36 |
NG_012004.1:g.33985G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.2615-269G>A MANE Select | ENSP00000263923.4:n.2615-269G>A | |
ENST00000647068.1:n.2628-269G>A | ||
ENST00000263923.4:c.2615-269G>A | ENSP00000263923.4:n.2615-269G>A | |
ENST00000509309.1:n.110G>A | ||
NM_002253.2:c.2615-269G>A | NP_002244.1:n.2615-269G>A | |
NM_002253.3:c.2615-269G>A | NP_002244.1:n.2615-269G>A | |
NM_002253.4:c.2615-269G>A MANE Select | NP_002244.1:n.2615-269G>A |