Canonical Allele Identifier: CA346670944

Gene: ABCG8

Linked Data

• dbSNP Id: rs1670005264
• MyVariant Identifiers: chr2:g.44104790C>T (hg19) ; chr2:g.43877651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877651C>T , CM000664.2:g.43877651C>T	GRCh38
NC_000002.11:g.44104790C>T , CM000664.1:g.44104790C>T	GRCh37
NC_000002.10:g.43958294C>T	NCBI36
NG_008884.1:g.43688C>T
NG_008884.2:g.50710C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1847C>T MANE Select	ENSP00000272286.2:p.Pro616Leu
ENST00000272286.2:c.1847C>T	ENSP00000272286.2:p.Pro616Leu
NM_022437.2:c.1847C>T	NP_071882.1:p.Pro616Leu
XM_005264483.2:c.1844C>T	XP_005264540.1:p.Pro615Leu
XM_011533029.1:c.1859C>T	XP_011531331.1:p.Pro620Leu
XM_011533030.1:c.1856C>T	XP_011531332.1:p.Pro619Leu
XM_011533031.1:c.1631C>T	XP_011531333.1:p.Pro544Leu
XR_939707.1:n.2349C>T
NM_001357321.1:c.1844C>T	NP_001344250.1:p.Pro615Leu
XM_011533029.2:c.1859C>T	XP_011531331.1:p.Pro620Leu
XM_011533030.2:c.1856C>T	XP_011531332.1:p.Pro619Leu
XR_001738891.1:n.2363C>T
XR_939707.2:n.2363C>T
NM_022437.3:c.1847C>T MANE Select	NP_071882.1:p.Pro616Leu
NM_001357321.2:c.1844C>T	NP_001344250.1:p.Pro615Leu