Canonical Allele Identifier: CA2176240363
Gene: ATP8B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50140172T= , CM000677.2:g.50140172T= GRCh38
NC_000015.9:g.50432369T= , CM000677.1:g.50432369T= GRCh37
NC_000015.8:g.48219661T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000558829.1:c.-42-33164A= ENSP00000453539.1:n.-42-33164A=
XM_011522056.1:c.-42-33164A= XP_011520358.1:n.-42-33164A=
XM_011522056.3:c.-42-33164A= XP_011520358.3:n.-42-33164A=
XM_017022587.2:c.-42-33164A= XP_016878076.2:n.-42-33164A=