Canonical Allele Identifier: CA2176240362
Gene: ATP8B4 HGNC NCBI

Linked Data

dbSNP Id: rs2044187907
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50140171A>G , CM000677.2:g.50140171A>G GRCh38
NC_000015.9:g.50432368A>G , CM000677.1:g.50432368A>G GRCh37
NC_000015.8:g.48219660A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000558829.1:c.-42-33163T>C ENSP00000453539.1:n.-42-33163T>C
XM_011522056.1:c.-42-33163T>C XP_011520358.1:n.-42-33163T>C
XM_011522056.3:c.-42-33163T>C XP_011520358.3:n.-42-33163T>C
XM_017022587.2:c.-42-33163T>C XP_016878076.2:n.-42-33163T>C
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