Canonical Allele Identifier: CA346662569

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43839102-C-G
• MyVariant Identifiers: chr2:g.44066241C>G (hg19) ; chr2:g.43839102C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43839102C>G , CM000664.2:g.43839102C>G	GRCh38
NC_000002.11:g.44066241C>G , CM000664.1:g.44066241C>G	GRCh37
NC_000002.10:g.43919745C>G	NCBI36
NG_008883.1:g.4718G>C
NG_008884.1:g.5139C>G
NG_008884.2:g.12161C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.49C>G MANE Select	ENSP00000272286.2:p.Pro17Ala
ENST00000643284.1:n.521-5405C>G
ENST00000644611.1:c.76-5405C>G	ENSP00000495423.1:n.76-5405C>G
ENST00000272286.2:c.49C>G	ENSP00000272286.2:p.Pro17Ala
NM_022437.2:c.49C>G	NP_071882.1:p.Pro17Ala
XM_005264483.2:c.49C>G	XP_005264540.1:p.Pro17Ala
XM_011533029.1:c.76-5405C>G	XP_011531331.1:n.76-5405C>G
XM_011533030.1:c.76-5405C>G	XP_011531332.1:n.76-5405C>G
XM_011533031.1:c.-153-5405C>G	XP_011531333.1:n.-153-5405C>G
XR_939707.1:n.566-5405C>G
NM_001357321.1:c.49C>G	NP_001344250.1:p.Pro17Ala
XM_011533029.2:c.76-5405C>G	XP_011531331.1:n.76-5405C>G
XM_011533030.2:c.76-5405C>G	XP_011531332.1:n.76-5405C>G
XR_001738891.1:n.580-5405C>G
XR_939707.2:n.580-5405C>G
NM_022437.3:c.49C>G MANE Select	NP_071882.1:p.Pro17Ala
NM_001357321.2:c.49C>G	NP_001344250.1:p.Pro17Ala