Canonical Allele Identifier: CA617859691
Gene: ATP8B4 HGNC NCBI

Linked Data

dbSNP Id: rs1406569285
gnomAD v2: 15-50432532-C-T
gnomAD v3: 15-50140335-C-T
gnomAD v4: 15-50140335-C-T
MyVariant Identifiers: chr15:g.50432532C>T (hg19) chr15:g.50140335C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50140335C>T , CM000677.2:g.50140335C>T GRCh38
NC_000015.9:g.50432532C>T , CM000677.1:g.50432532C>T GRCh37
NC_000015.8:g.48219824C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558829.1:c.-42-33327G>A ENSP00000453539.1:n.-42-33327G>A
XM_011522056.1:c.-42-33327G>A XP_011520358.1:n.-42-33327G>A
XM_011522056.3:c.-42-33327G>A XP_011520358.3:n.-42-33327G>A
XM_017022587.2:c.-42-33327G>A XP_016878076.2:n.-42-33327G>A
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