HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55096603T>C , CM000666.2:g.55096603T>C | GRCh38 |
NC_000004.11:g.55962770T>C , CM000666.1:g.55962770T>C | GRCh37 |
NC_000004.10:g.55657527T>C | NCBI36 |
NG_012004.1:g.33993A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.2615-261A>G MANE Select | ENSP00000263923.4:n.2615-261A>G | |
ENST00000647068.1:n.2628-261A>G | ||
ENST00000263923.4:c.2615-261A>G | ENSP00000263923.4:n.2615-261A>G | |
ENST00000509309.1:n.118A>G | ||
NM_002253.2:c.2615-261A>G | NP_002244.1:n.2615-261A>G | |
NM_002253.3:c.2615-261A>G | NP_002244.1:n.2615-261A>G | |
NM_002253.4:c.2615-261A>G MANE Select | NP_002244.1:n.2615-261A>G |