Canonical Allele Identifier: CA2176240434
Gene: ATP8B4 HGNC NCBI

Linked Data

dbSNP Id: rs2044189882

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50140340G>A , CM000677.2:g.50140340G>A GRCh38
NC_000015.9:g.50432537G>A , CM000677.1:g.50432537G>A GRCh37
NC_000015.8:g.48219829G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558829.1:c.-42-33332C>T ENSP00000453539.1:n.-42-33332C>T
XM_011522056.1:c.-42-33332C>T XP_011520358.1:n.-42-33332C>T
XM_011522056.3:c.-42-33332C>T XP_011520358.3:n.-42-33332C>T
XM_017022587.2:c.-42-33332C>T XP_016878076.2:n.-42-33332C>T