Canonical Allele Identifier: CA504874563
Gene: BSG HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.580403A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.580403A>C , CM000681.2:g.580403A>C GRCh38
NC_000019.9:g.580403A>C , CM000681.1:g.580403A>C GRCh37
NC_000019.8:g.531403A>C NCBI36
NG_007468.1:g.14079A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333511.9:c.597A>C MANE Select ENSP00000333769.3:p.Gly199=
ENST00000346916.9:c.-31A>C ENSP00000344707.4:n.-31A>C
ENST00000353555.9:c.249A>C ENSP00000343809.4:p.Gly83=
ENST00000571735.3:n.832A>C
ENST00000572899.6:n.290A>C
ENST00000573784.6:c.-31A>C ENSP00000473393.2:n.-31A>C
ENST00000576925.4:n.1034A>C
ENST00000576984.3:c.-31A>C ENSP00000473528.2:n.-31A>C
ENST00000613627.5:c.92A>C ENSP00000484849.2:p.Glu31Ala
ENST00000618112.4:c.249A>C ENSP00000495088.2:p.Gly83=
ENST00000679472.1:c.-31A>C ENSP00000505067.1:n.-31A>C
ENST00000680065.1:c.-31A>C ENSP00000506020.1:n.-31A>C
ENST00000680326.1:c.240A>C ENSP00000505863.1:p.Gly80=
ENST00000680552.1:c.249A>C ENSP00000506321.1:p.Gly83=
ENST00000333511.7:c.597A>C ENSP00000333769.3:p.Gly199=
ENST00000346916.8:c.57A>C ENSP00000344707.3:p.Gly19=
ENST00000353555.8:c.249A>C ENSP00000343809.4:p.Gly83=
ENST00000545507.6:c.-31A>C ENSP00000473664.1:n.-31A>C
ENST00000571735.2:n.846A>C
ENST00000572899.5:n.290A>C
ENST00000573216.5:c.225A>C ENSP00000458665.1:p.Gly75=
ENST00000573784.5:c.-31A>C ENSP00000473393.1:n.-31A>C
ENST00000576984.2:c.-31A>C ENSP00000473528.1:n.-31A>C
ENST00000613627.4:c.240A>C ENSP00000484849.1:p.Gly80=
ENST00000614867.2:c.147+824A>C ENSP00000484624.1:n.147+824A>C
ENST00000618006.4:c.68-243A>C ENSP00000478958.1:n.68-243A>C
NM_001728.3:c.597A>C NP_001719.2:p.Gly199=
NM_198589.2:c.249A>C NP_940991.1:p.Gly83=
NM_198590.2:c.-31A>C NP_940992.1:n.-31A>C
NM_198591.2:c.57A>C NP_940993.1:p.Gly19=
XM_005259619.1:c.249A>C XP_005259676.1:p.Gly83=
NM_001322243.1:c.249A>C NP_001309172.1:p.Gly83=
XM_017027173.2:c.597A>C XP_016882662.1:p.Gly199=
NM_001322243.2:c.249A>C NP_001309172.1:p.Gly83=
NM_001728.4:c.597A>C MANE Select NP_001719.2:p.Gly199=
NM_198589.3:c.249A>C NP_940991.1:p.Gly83=
NM_198590.3:c.-31A>C NP_940992.1:n.-31A>C
NM_198591.3:c.57A>C NP_940993.1:p.Gly19=
NM_198591.4:c.-31A>C NP_940993.2:n.-31A>C