Canonical Allele Identifier: CA346671237

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104940C>G (hg19) ; chr2:g.43877801C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877801C>G , CM000664.2:g.43877801C>G	GRCh38
NC_000002.11:g.44104940C>G , CM000664.1:g.44104940C>G	GRCh37
NC_000002.10:g.43958444C>G	NCBI36
NG_008884.1:g.43838C>G
NG_008884.2:g.50860C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1910C>G MANE Select	ENSP00000272286.2:p.Ser637Trp
ENST00000272286.2:c.1910C>G	ENSP00000272286.2:p.Ser637Trp
NM_022437.2:c.1910C>G	NP_071882.1:p.Ser637Trp
XM_005264483.2:c.1907C>G	XP_005264540.1:p.Ser636Trp
XM_011533029.1:c.1922C>G	XP_011531331.1:p.Ser641Trp
XM_011533030.1:c.1919C>G	XP_011531332.1:p.Ser640Trp
XM_011533031.1:c.1694C>G	XP_011531333.1:p.Ser565Trp
XR_939707.1:n.2412C>G
NM_001357321.1:c.1907C>G	NP_001344250.1:p.Ser636Trp
XM_011533029.2:c.1922C>G	XP_011531331.1:p.Ser641Trp
XM_011533030.2:c.1919C>G	XP_011531332.1:p.Ser640Trp
XR_001738891.1:n.2426C>G
XR_939707.2:n.2426C>G
NM_022437.3:c.1910C>G MANE Select	NP_071882.1:p.Ser637Trp
NM_001357321.2:c.1907C>G	NP_001344250.1:p.Ser636Trp