Canonical Allele Identifier: CA2658820506

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43838966-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43838966C>T , CM000664.2:g.43838966C>T	GRCh38
NC_000002.11:g.44066105C>T , CM000664.1:g.44066105C>T	GRCh37
NC_000002.10:g.43919609C>T	NCBI36
NG_008883.1:g.4854G>A
NG_008884.1:g.5003C>T
NG_008884.2:g.12025C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643284.1:n.521-5541C>T
ENST00000644611.1:c.76-5541C>T	ENSP00000495423.1:n.76-5541C>T
ENST00000272286.2:c.-88C>T	ENSP00000272286.2:n.-88C>T
NM_022437.2:c.-88C>T	NP_071882.1:n.-88C>T
XM_005264483.2:c.-88C>T	XP_005264540.1:n.-88C>T
XM_011533029.1:c.76-5541C>T	XP_011531331.1:n.76-5541C>T
XM_011533030.1:c.76-5541C>T	XP_011531332.1:n.76-5541C>T
XM_011533031.1:c.-153-5541C>T	XP_011531333.1:n.-153-5541C>T
XR_939707.1:n.566-5541C>T
NM_001357321.1:c.-88C>T	NP_001344250.1:n.-88C>T
XM_011533029.2:c.76-5541C>T	XP_011531331.1:n.76-5541C>T
XM_011533030.2:c.76-5541C>T	XP_011531332.1:n.76-5541C>T
XR_001738891.1:n.580-5541C>T
XR_939707.2:n.580-5541C>T