Canonical Allele Identifier: CA2176240352
Gene: ATP8B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50140147G= , CM000677.2:g.50140147G= GRCh38
NC_000015.9:g.50432344G= , CM000677.1:g.50432344G= GRCh37
NC_000015.8:g.48219636G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558829.1:c.-42-33139C= ENSP00000453539.1:n.-42-33139C=
XM_011522056.1:c.-42-33139C= XP_011520358.1:n.-42-33139C=
XM_011522056.3:c.-42-33139C= XP_011520358.3:n.-42-33139C=
XM_017022587.2:c.-42-33139C= XP_016878076.2:n.-42-33139C=