Canonical Allele Identifier: CA97374098
Gene:

Linked Data

dbSNP Id: rs973026168
MyVariant Identifiers: chr4:g.54072409A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072409A>T , CM000666.2:g.54072409A>T GRCh38
NC_000004.11:g.54938576A>T , CM000666.1:g.54938576A>T GRCh37
NC_000004.10:g.54633333A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202516A>T ENSP00000423325.1:n.1018-202516A>T
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