Canonical Allele Identifier: CA402858497

Gene: BSG

Linked Data

• MyVariant Identifiers: chr19:g.580432C>A (hg19) ; chr19:g.580432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.580432C>A , CM000681.2:g.580432C>A	GRCh38
NC_000019.9:g.580432C>A , CM000681.1:g.580432C>A	GRCh37
NC_000019.8:g.531432C>A	NCBI36
NG_007468.1:g.14108C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333511.9:c.626C>A MANE Select	ENSP00000333769.3:p.Pro209His
ENST00000346916.9:c.-2C>A	ENSP00000344707.4:n.-2C>A
ENST00000353555.9:c.278C>A	ENSP00000343809.4:p.Pro93His
ENST00000571735.3:n.861C>A
ENST00000572899.6:n.319C>A
ENST00000573784.6:c.-2C>A	ENSP00000473393.2:n.-2C>A
ENST00000576925.4:n.1063C>A
ENST00000576984.3:c.-2C>A	ENSP00000473528.2:n.-2C>A
ENST00000613627.5:c.121C>A	ENSP00000484849.2:p.Pro41Thr
ENST00000618112.4:c.278C>A	ENSP00000495088.2:p.Pro93His
ENST00000679472.1:c.-2C>A	ENSP00000505067.1:n.-2C>A
ENST00000680065.1:c.-2C>A	ENSP00000506020.1:n.-2C>A
ENST00000680326.1:c.269C>A	ENSP00000505863.1:p.Pro90His
ENST00000680552.1:c.278C>A	ENSP00000506321.1:p.Pro93His
ENST00000333511.7:c.626C>A	ENSP00000333769.3:p.Pro209His
ENST00000346916.8:c.86C>A	ENSP00000344707.3:p.Pro29His
ENST00000353555.8:c.278C>A	ENSP00000343809.4:p.Pro93His
ENST00000545507.6:c.-2C>A	ENSP00000473664.1:n.-2C>A
ENST00000571735.2:n.875C>A
ENST00000572899.5:n.319C>A
ENST00000573216.5:c.254C>A	ENSP00000458665.1:p.Pro85His
ENST00000573784.5:c.-2C>A	ENSP00000473393.1:n.-2C>A
ENST00000576984.2:c.-2C>A	ENSP00000473528.1:n.-2C>A
ENST00000613627.4:c.269C>A	ENSP00000484849.1:p.Pro90His
ENST00000614867.2:c.147+853C>A	ENSP00000484624.1:n.147+853C>A
ENST00000618006.4:c.68-214C>A	ENSP00000478958.1:n.68-214C>A
NM_001728.3:c.626C>A	NP_001719.2:p.Pro209His
NM_198589.2:c.278C>A	NP_940991.1:p.Pro93His
NM_198590.2:c.-2C>A	NP_940992.1:n.-2C>A
NM_198591.2:c.86C>A	NP_940993.1:p.Pro29His
XM_005259619.1:c.278C>A	XP_005259676.1:p.Pro93His
NM_001322243.1:c.278C>A	NP_001309172.1:p.Pro93His
XM_017027173.2:c.626C>A	XP_016882662.1:p.Pro209His
NM_001322243.2:c.278C>A	NP_001309172.1:p.Pro93His
NM_001728.4:c.626C>A MANE Select	NP_001719.2:p.Pro209His
NM_198589.3:c.278C>A	NP_940991.1:p.Pro93His
NM_198590.3:c.-2C>A	NP_940992.1:n.-2C>A
NM_198591.3:c.86C>A	NP_940993.1:p.Pro29His
NM_198591.4:c.-2C>A	NP_940993.2:n.-2C>A