Canonical Allele Identifier: CA2176240417
Gene: ATP8B4 HGNC NCBI

Linked Data

dbSNP Id: rs2044189432
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50140301T>C , CM000677.2:g.50140301T>C GRCh38
NC_000015.9:g.50432498T>C , CM000677.1:g.50432498T>C GRCh37
NC_000015.8:g.48219790T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000558829.1:c.-42-33293A>G ENSP00000453539.1:n.-42-33293A>G
XM_011522056.1:c.-42-33293A>G XP_011520358.1:n.-42-33293A>G
XM_011522056.3:c.-42-33293A>G XP_011520358.3:n.-42-33293A>G
XM_017022587.2:c.-42-33293A>G XP_016878076.2:n.-42-33293A>G
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