Canonical Allele Identifier: CA2584179668
Gene: BSG HGNC NCBI

Linked Data

gnomAD v4: 19-583004-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.583004G>A , CM000681.2:g.583004G>A GRCh38
NC_000019.9:g.583004G>A , CM000681.1:g.583004G>A GRCh37
NC_000019.8:g.534004G>A NCBI36
NG_007468.1:g.16680G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333511.9:c.*260G>A MANE Select ENSP00000333769.3:n.*260G>A
ENST00000346916.9:c.*260G>A ENSP00000344707.4:n.*260G>A
ENST00000353555.9:c.*260G>A ENSP00000343809.4:n.*260G>A
ENST00000571735.3:n.1653G>A
ENST00000573784.6:c.*260G>A ENSP00000473393.2:n.*260G>A
ENST00000576925.4:n.1855G>A
ENST00000576984.3:c.*260G>A ENSP00000473528.2:n.*260G>A
ENST00000618112.4:c.1060G>A ENSP00000495088.2:n.1060G>A
ENST00000679472.1:c.*166G>A ENSP00000505067.1:n.*166G>A
ENST00000680065.1:c.*256G>A ENSP00000506020.1:n.*256G>A
ENST00000680326.1:c.*260G>A ENSP00000505863.1:n.*260G>A
ENST00000680552.1:c.*260G>A ENSP00000506321.1:n.*260G>A
ENST00000333511.7:c.*260G>A ENSP00000333769.3:n.*260G>A
ENST00000346916.8:c.*260G>A ENSP00000344707.3:n.*260G>A
ENST00000353555.8:c.*260G>A ENSP00000343809.4:n.*260G>A
ENST00000545507.6:c.*260G>A ENSP00000473664.1:n.*260G>A
ENST00000571735.2:n.1667G>A
ENST00000614867.2:c.*297G>A ENSP00000484624.1:n.*297G>A
ENST00000618006.4:c.*260G>A ENSP00000478958.1:n.*260G>A
ENST00000618112.2:n.343G>A
NM_001728.3:c.*260G>A NP_001719.2:n.*260G>A
NM_198589.2:c.*260G>A NP_940991.1:n.*260G>A
NM_198590.2:c.*260G>A NP_940992.1:n.*260G>A
NM_198591.2:c.*260G>A NP_940993.1:n.*260G>A
XM_005259619.1:c.*256G>A XP_005259676.1:n.*256G>A
NM_001322243.1:c.*256G>A NP_001309172.1:n.*256G>A
XM_017027173.2:c.*256G>A XP_016882662.1:n.*256G>A
NM_001322243.2:c.*256G>A NP_001309172.1:n.*256G>A
NM_001728.4:c.*260G>A MANE Select NP_001719.2:n.*260G>A
NM_198589.3:c.*260G>A NP_940991.1:n.*260G>A
NM_198590.3:c.*260G>A NP_940992.1:n.*260G>A
NM_198591.3:c.*260G>A NP_940993.1:n.*260G>A
NM_198591.4:c.*260G>A NP_940993.2:n.*260G>A