Canonical Allele Identifier: CA270442261

Gene: ATP8B4

Linked Data

• dbSNP Id: rs887637919
• gnomAD v3: 15-50140151-G-A
• gnomAD v4: 15-50140151-G-A
• MyVariant Identifiers: chr15:g.50432348G>A (hg19) ; chr15:g.50140151G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50140151G>A , CM000677.2:g.50140151G>A	GRCh38
NC_000015.9:g.50432348G>A , CM000677.1:g.50432348G>A	GRCh37
NC_000015.8:g.48219640G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558829.1:c.-42-33143C>T	ENSP00000453539.1:n.-42-33143C>T
XM_011522056.1:c.-42-33143C>T	XP_011520358.1:n.-42-33143C>T
XM_011522056.3:c.-42-33143C>T	XP_011520358.3:n.-42-33143C>T
XM_017022587.2:c.-42-33143C>T	XP_016878076.2:n.-42-33143C>T