Canonical Allele Identifier: CA346670959

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104799A>C (hg19) ; chr2:g.43877660A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877660A>C , CM000664.2:g.43877660A>C	GRCh38
NC_000002.11:g.44104799A>C , CM000664.1:g.44104799A>C	GRCh37
NC_000002.10:g.43958303A>C	NCBI36
NG_008884.1:g.43697A>C
NG_008884.2:g.50719A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1856A>C MANE Select	ENSP00000272286.2:p.Asn619Thr
ENST00000272286.2:c.1856A>C	ENSP00000272286.2:p.Asn619Thr
NM_022437.2:c.1856A>C	NP_071882.1:p.Asn619Thr
XM_005264483.2:c.1853A>C	XP_005264540.1:p.Asn618Thr
XM_011533029.1:c.1868A>C	XP_011531331.1:p.Asn623Thr
XM_011533030.1:c.1865A>C	XP_011531332.1:p.Asn622Thr
XM_011533031.1:c.1640A>C	XP_011531333.1:p.Asn547Thr
XR_939707.1:n.2358A>C
NM_001357321.1:c.1853A>C	NP_001344250.1:p.Asn618Thr
XM_011533029.2:c.1868A>C	XP_011531331.1:p.Asn623Thr
XM_011533030.2:c.1865A>C	XP_011531332.1:p.Asn622Thr
XR_001738891.1:n.2372A>C
XR_939707.2:n.2372A>C
NM_022437.3:c.1856A>C MANE Select	NP_071882.1:p.Asn619Thr
NM_001357321.2:c.1853A>C	NP_001344250.1:p.Asn618Thr