Canonical Allele Identifier: CA2317191011

Gene: BSG

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.582927T>C , CM000681.2:g.582927T>C	GRCh38
NC_000019.9:g.582927T>C , CM000681.1:g.582927T>C	GRCh37
NC_000019.8:g.533927T>C	NCBI36
NG_007468.1:g.16603T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333511.9:c.*183T>C MANE Select	ENSP00000333769.3:n.*183T>C
ENST00000346916.9:c.*183T>C	ENSP00000344707.4:n.*183T>C
ENST00000353555.9:c.*183T>C	ENSP00000343809.4:n.*183T>C
ENST00000571735.3:n.1576T>C
ENST00000573784.6:c.*183T>C	ENSP00000473393.2:n.*183T>C
ENST00000576925.4:n.1778T>C
ENST00000576984.3:c.*183T>C	ENSP00000473528.2:n.*183T>C
ENST00000618112.4:c.983T>C	ENSP00000495088.2:n.983T>C
ENST00000679472.1:c.*89T>C	ENSP00000505067.1:n.*89T>C
ENST00000680065.1:c.*179T>C	ENSP00000506020.1:n.*179T>C
ENST00000680326.1:c.*183T>C	ENSP00000505863.1:n.*183T>C
ENST00000680552.1:c.*183T>C	ENSP00000506321.1:n.*183T>C
ENST00000333511.7:c.*183T>C	ENSP00000333769.3:n.*183T>C
ENST00000346916.8:c.*183T>C	ENSP00000344707.3:n.*183T>C
ENST00000353555.8:c.*183T>C	ENSP00000343809.4:n.*183T>C
ENST00000545507.6:c.*183T>C	ENSP00000473664.1:n.*183T>C
ENST00000571735.2:n.1590T>C
ENST00000614867.2:c.*220T>C	ENSP00000484624.1:n.*220T>C
ENST00000618006.4:c.*183T>C	ENSP00000478958.1:n.*183T>C
ENST00000618112.2:n.266T>C
NM_001728.3:c.*183T>C	NP_001719.2:n.*183T>C
NM_198589.2:c.*183T>C	NP_940991.1:n.*183T>C
NM_198590.2:c.*183T>C	NP_940992.1:n.*183T>C
NM_198591.2:c.*183T>C	NP_940993.1:n.*183T>C
XM_005259619.1:c.*179T>C	XP_005259676.1:n.*179T>C
NM_001322243.1:c.*179T>C	NP_001309172.1:n.*179T>C
XM_017027173.2:c.*179T>C	XP_016882662.1:n.*179T>C
NM_001322243.2:c.*179T>C	NP_001309172.1:n.*179T>C
NM_001728.4:c.*183T>C MANE Select	NP_001719.2:n.*183T>C
NM_198589.3:c.*183T>C	NP_940991.1:n.*183T>C
NM_198590.3:c.*183T>C	NP_940992.1:n.*183T>C
NM_198591.3:c.*183T>C	NP_940993.1:n.*183T>C
NM_198591.4:c.*183T>C	NP_940993.2:n.*183T>C