Canonical Allele Identifier: CA1637475

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43874497G>T , CM000664.2:g.43874497G>T	GRCh38
NC_000002.11:g.44101636G>T , CM000664.1:g.44101636G>T	GRCh37
NC_000002.10:g.43955140G>T	NCBI36
NG_008884.1:g.40534G>T
NG_008884.2:g.47556G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022437.3:c.1488+14G>T MANE Select	NP_071882.1:n.1488+14G>T
ENST00000272286.4:c.1488+14G>T MANE Select	ENSP00000272286.2:n.1488+14G>T
NM_001357321.1:c.1485+14G>T	NP_001344250.1:n.1485+14G>T
NM_001357321.2:c.1485+14G>T	NP_001344250.1:n.1485+14G>T
NM_022437.2:c.1488+14G>T	NP_071882.1:n.1488+14G>T
ENST00000272286.2:c.1488+14G>T	ENSP00000272286.2:n.1488+14G>T
XM_005264483.2:c.1485+14G>T	XP_005264540.1:n.1485+14G>T
XM_011533029.1:c.1500+14G>T	XP_011531331.1:n.1500+14G>T
XM_011533029.2:c.1500+14G>T	XP_011531331.1:n.1500+14G>T
XM_011533030.1:c.1497+14G>T	XP_011531332.1:n.1497+14G>T
XM_011533030.2:c.1497+14G>T	XP_011531332.1:n.1497+14G>T
XM_011533031.1:c.1272+14G>T	XP_011531333.1:n.1272+14G>T
XR_001738891.1:n.2004+14G>T
XR_939707.1:n.1990+14G>T
XR_939707.2:n.2004+14G>T