Canonical Allele Identifier: CA1637695

Gene: ABCG8

Linked Data

• dbSNP Id: rs753262274
• ExAC: 2:44104835 G / A
• gnomAD v2: 2-44104835-G-A
• gnomAD v3: 2-43877696-G-A
• gnomAD v4: 2-43877696-G-A
• MyVariant Identifiers: chr2:g.44104835G>A (hg19) ; chr2:g.43877696G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877696G>A , CM000664.2:g.43877696G>A	GRCh38
NC_000002.11:g.44104835G>A , CM000664.1:g.44104835G>A	GRCh37
NC_000002.10:g.43958339G>A	NCBI36
NG_008884.1:g.43733G>A
NG_008884.2:g.50755G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.1884+8G>A MANE Select	ENSP00000272286.2:n.1884+8G>A
ENST00000272286.2:c.1884+8G>A	ENSP00000272286.2:n.1884+8G>A
NM_022437.2:c.1884+8G>A	NP_071882.1:n.1884+8G>A
XM_005264483.2:c.1881+8G>A	XP_005264540.1:n.1881+8G>A
XM_011533029.1:c.1896+8G>A	XP_011531331.1:n.1896+8G>A
XM_011533030.1:c.1893+8G>A	XP_011531332.1:n.1893+8G>A
XM_011533031.1:c.1668+8G>A	XP_011531333.1:n.1668+8G>A
XR_939707.1:n.2386+8G>A
NM_001357321.1:c.1881+8G>A	NP_001344250.1:n.1881+8G>A
XM_011533029.2:c.1896+8G>A	XP_011531331.1:n.1896+8G>A
XM_011533030.2:c.1893+8G>A	XP_011531332.1:n.1893+8G>A
XR_001738891.1:n.2400+8G>A
XR_939707.2:n.2400+8G>A
NM_022437.3:c.1884+8G>A MANE Select	NP_071882.1:n.1884+8G>A
NM_001357321.2:c.1881+8G>A	NP_001344250.1:n.1881+8G>A