Canonical Allele Identifier: CA346663619

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44073407C>A (hg19) ; chr2:g.43846268C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846268C>A , CM000664.2:g.43846268C>A	GRCh38
NC_000002.11:g.44073407C>A , CM000664.1:g.44073407C>A	GRCh37
NC_000002.10:g.43926911C>A	NCBI36
NG_008884.1:g.12305C>A
NG_008884.2:g.19327C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.279C>A MANE Select	ENSP00000272286.2:p.Phe93Leu
ENST00000643284.1:n.736C>A
ENST00000644611.1:c.291C>A	ENSP00000495423.1:p.Phe97Leu
ENST00000272286.2:c.279C>A	ENSP00000272286.2:p.Phe93Leu
NM_022437.2:c.279C>A	NP_071882.1:p.Phe93Leu
XM_005264483.2:c.279C>A	XP_005264540.1:p.Phe93Leu
XM_011533029.1:c.291C>A	XP_011531331.1:p.Phe97Leu
XM_011533030.1:c.291C>A	XP_011531332.1:p.Phe97Leu
XM_011533031.1:c.63C>A	XP_011531333.1:p.Phe21Leu
XR_939707.1:n.781C>A
NM_001357321.1:c.279C>A	NP_001344250.1:p.Phe93Leu
XM_011533029.2:c.291C>A	XP_011531331.1:p.Phe97Leu
XM_011533030.2:c.291C>A	XP_011531332.1:p.Phe97Leu
XR_001738891.1:n.795C>A
XR_939707.2:n.795C>A
NM_022437.3:c.279C>A MANE Select	NP_071882.1:p.Phe93Leu
NM_001357321.2:c.279C>A	NP_001344250.1:p.Phe93Leu