Canonical Allele Identifier: CA425908298

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104947T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877808T>C , CM000664.2:g.43877808T>C	GRCh38
NC_000002.11:g.44104947T>C , CM000664.1:g.44104947T>C	GRCh37
NC_000002.10:g.43958451T>C	NCBI36
NG_008884.1:g.43845T>C
NG_008884.2:g.50867T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.1917T>C MANE Select	ENSP00000272286.2:p.Pro639=
ENST00000272286.2:c.1917T>C	ENSP00000272286.2:p.Pro639=
NM_022437.2:c.1917T>C	NP_071882.1:p.Pro639=
XM_005264483.2:c.1914T>C	XP_005264540.1:p.Pro638=
XM_011533029.1:c.1929T>C	XP_011531331.1:p.Pro643=
XM_011533030.1:c.1926T>C	XP_011531332.1:p.Pro642=
XM_011533031.1:c.1701T>C	XP_011531333.1:p.Pro567=
XR_939707.1:n.2419T>C
NM_001357321.1:c.1914T>C	NP_001344250.1:p.Pro638=
XM_011533029.2:c.1929T>C	XP_011531331.1:p.Pro643=
XM_011533030.2:c.1926T>C	XP_011531332.1:p.Pro642=
XR_001738891.1:n.2433T>C
XR_939707.2:n.2433T>C
NM_022437.3:c.1917T>C MANE Select	NP_071882.1:p.Pro639=
NM_001357321.2:c.1914T>C	NP_001344250.1:p.Pro638=