Canonical Allele Identifier: CA425908326

Gene: ABCG8

Linked Data

• dbSNP Id: rs1670015065
• gnomAD v4: 2-43877847-T-C
• MyVariant Identifiers: chr2:g.44104986T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877847T>C , CM000664.2:g.43877847T>C	GRCh38
NC_000002.11:g.44104986T>C , CM000664.1:g.44104986T>C	GRCh37
NC_000002.10:g.43958490T>C	NCBI36
NG_008884.1:g.43884T>C
NG_008884.2:g.50906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1956T>C MANE Select	ENSP00000272286.2:p.Gly652=
ENST00000272286.2:c.1956T>C	ENSP00000272286.2:p.Gly652=
NM_022437.2:c.1956T>C	NP_071882.1:p.Gly652=
XM_005264483.2:c.1953T>C	XP_005264540.1:p.Gly651=
XM_011533029.1:c.1968T>C	XP_011531331.1:p.Gly656=
XM_011533030.1:c.1965T>C	XP_011531332.1:p.Gly655=
XM_011533031.1:c.1740T>C	XP_011531333.1:p.Gly580=
XR_939707.1:n.2458T>C
NM_001357321.1:c.1953T>C	NP_001344250.1:p.Gly651=
XM_011533029.2:c.1968T>C	XP_011531331.1:p.Gly656=
XM_011533030.2:c.1965T>C	XP_011531332.1:p.Gly655=
XR_001738891.1:n.2472T>C
XR_939707.2:n.2472T>C
NM_022437.3:c.1956T>C MANE Select	NP_071882.1:p.Gly652=
NM_001357321.2:c.1953T>C	NP_001344250.1:p.Gly651=