HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17118389C>A , CM000663.2:g.17118389C>A | GRCh38 |
NC_000001.10:g.17444884C>A , CM000663.1:g.17444884C>A | GRCh37 |
NC_000001.9:g.17317471C>A | NCBI36 |
NG_033958.1:g.6065G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375486.9:c.92+891G>T MANE Select | ENSP00000364635.4:n.92+891G>T | |
ENST00000375481.1:c.92+891G>T | ENSP00000364630.1:n.92+891G>T | |
ENST00000375486.8:c.92+891G>T | ENSP00000364635.4:n.92+891G>T | |
NM_007365.2:c.92+891G>T | NP_031391.2:n.92+891G>T | |
XM_011540549.1:c.92+891G>T | XP_011538851.1:n.92+891G>T | |
XR_947004.1:n.4965C>A | ||
XR_001736944.1:n.174+891G>T | ||
NM_007365.3:c.92+891G>T MANE Select | NP_031391.2:n.92+891G>T |