Canonical Allele Identifier: CA346671510

Gene: ABCG8

Linked Data

• dbSNP Id: rs1670016016
• gnomAD v3: 2-43877881-T-C
• gnomAD v4: 2-43877881-T-C
• MyVariant Identifiers: chr2:g.44105020T>C (hg19) ; chr2:g.43877881T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877881T>C , CM000664.2:g.43877881T>C	GRCh38
NC_000002.11:g.44105020T>C , CM000664.1:g.44105020T>C	GRCh37
NC_000002.10:g.43958524T>C	NCBI36
NG_008884.1:g.43918T>C
NG_008884.2:g.50940T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1990T>C MANE Select	ENSP00000272286.2:p.Phe664Leu
ENST00000272286.2:c.1990T>C	ENSP00000272286.2:p.Phe664Leu
NM_022437.2:c.1990T>C	NP_071882.1:p.Phe664Leu
XM_005264483.2:c.1987T>C	XP_005264540.1:p.Phe663Leu
XM_011533029.1:c.2002T>C	XP_011531331.1:p.Phe668Leu
XM_011533030.1:c.1999T>C	XP_011531332.1:p.Phe667Leu
XM_011533031.1:c.1774T>C	XP_011531333.1:p.Phe592Leu
XR_939707.1:n.2492T>C
NM_001357321.1:c.1987T>C	NP_001344250.1:p.Phe663Leu
XM_011533029.2:c.2002T>C	XP_011531331.1:p.Phe668Leu
XM_011533030.2:c.1999T>C	XP_011531332.1:p.Phe667Leu
XR_001738891.1:n.2506T>C
XR_939707.2:n.2506T>C
NM_022437.3:c.1990T>C MANE Select	NP_071882.1:p.Phe664Leu
NM_001357321.2:c.1987T>C	NP_001344250.1:p.Phe663Leu