Canonical Allele Identifier: CA346671345

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104968C>G (hg19) ; chr2:g.43877829C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877829C>G , CM000664.2:g.43877829C>G	GRCh38
NC_000002.11:g.44104968C>G , CM000664.1:g.44104968C>G	GRCh37
NC_000002.10:g.43958472C>G	NCBI36
NG_008884.1:g.43866C>G
NG_008884.2:g.50888C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1938C>G MANE Select	ENSP00000272286.2:p.Ile646Met
ENST00000272286.2:c.1938C>G	ENSP00000272286.2:p.Ile646Met
NM_022437.2:c.1938C>G	NP_071882.1:p.Ile646Met
XM_005264483.2:c.1935C>G	XP_005264540.1:p.Ile645Met
XM_011533029.1:c.1950C>G	XP_011531331.1:p.Ile650Met
XM_011533030.1:c.1947C>G	XP_011531332.1:p.Ile649Met
XM_011533031.1:c.1722C>G	XP_011531333.1:p.Ile574Met
XR_939707.1:n.2440C>G
NM_001357321.1:c.1935C>G	NP_001344250.1:p.Ile645Met
XM_011533029.2:c.1950C>G	XP_011531331.1:p.Ile650Met
XM_011533030.2:c.1947C>G	XP_011531332.1:p.Ile649Met
XR_001738891.1:n.2454C>G
XR_939707.2:n.2454C>G
NM_022437.3:c.1938C>G MANE Select	NP_071882.1:p.Ile646Met
NM_001357321.2:c.1935C>G	NP_001344250.1:p.Ile645Met