Canonical Allele Identifier: CA402858392

Gene: BSG

Linked Data

• gnomAD v4: 19-580402-G-T
• MyVariant Identifiers: chr19:g.580402G>T (hg19) ; chr19:g.580402G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.580402G>T , CM000681.2:g.580402G>T	GRCh38
NC_000019.9:g.580402G>T , CM000681.1:g.580402G>T	GRCh37
NC_000019.8:g.531402G>T	NCBI36
NG_007468.1:g.14078G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333511.9:c.596G>T MANE Select	ENSP00000333769.3:p.Gly199Val
ENST00000346916.9:c.-32G>T	ENSP00000344707.4:n.-32G>T
ENST00000353555.9:c.248G>T	ENSP00000343809.4:p.Gly83Val
ENST00000571735.3:n.831G>T
ENST00000572899.6:n.289G>T
ENST00000573784.6:c.-32G>T	ENSP00000473393.2:n.-32G>T
ENST00000576925.4:n.1033G>T
ENST00000576984.3:c.-32G>T	ENSP00000473528.2:n.-32G>T
ENST00000613627.5:c.91G>T	ENSP00000484849.2:p.Glu31Ter
ENST00000618112.4:c.248G>T	ENSP00000495088.2:p.Gly83Val
ENST00000679472.1:c.-32G>T	ENSP00000505067.1:n.-32G>T
ENST00000680065.1:c.-32G>T	ENSP00000506020.1:n.-32G>T
ENST00000680326.1:c.239G>T	ENSP00000505863.1:p.Gly80Val
ENST00000680552.1:c.248G>T	ENSP00000506321.1:p.Gly83Val
ENST00000333511.7:c.596G>T	ENSP00000333769.3:p.Gly199Val
ENST00000346916.8:c.56G>T	ENSP00000344707.3:p.Gly19Val
ENST00000353555.8:c.248G>T	ENSP00000343809.4:p.Gly83Val
ENST00000545507.6:c.-32G>T	ENSP00000473664.1:n.-32G>T
ENST00000571735.2:n.845G>T
ENST00000572899.5:n.289G>T
ENST00000573216.5:c.224G>T	ENSP00000458665.1:p.Gly75Val
ENST00000573784.5:c.-32G>T	ENSP00000473393.1:n.-32G>T
ENST00000576984.2:c.-32G>T	ENSP00000473528.1:n.-32G>T
ENST00000613627.4:c.239G>T	ENSP00000484849.1:p.Gly80Val
ENST00000614867.2:c.147+823G>T	ENSP00000484624.1:n.147+823G>T
ENST00000618006.4:c.68-244G>T	ENSP00000478958.1:n.68-244G>T
NM_001728.3:c.596G>T	NP_001719.2:p.Gly199Val
NM_198589.2:c.248G>T	NP_940991.1:p.Gly83Val
NM_198590.2:c.-32G>T	NP_940992.1:n.-32G>T
NM_198591.2:c.56G>T	NP_940993.1:p.Gly19Val
XM_005259619.1:c.248G>T	XP_005259676.1:p.Gly83Val
NM_001322243.1:c.248G>T	NP_001309172.1:p.Gly83Val
XM_017027173.2:c.596G>T	XP_016882662.1:p.Gly199Val
NM_001322243.2:c.248G>T	NP_001309172.1:p.Gly83Val
NM_001728.4:c.596G>T MANE Select	NP_001719.2:p.Gly199Val
NM_198589.3:c.248G>T	NP_940991.1:p.Gly83Val
NM_198590.3:c.-32G>T	NP_940992.1:n.-32G>T
NM_198591.3:c.56G>T	NP_940993.1:p.Gly19Val
NM_198591.4:c.-32G>T	NP_940993.2:n.-32G>T