Canonical Allele Identifier: CA788493083
Gene:

Linked Data

dbSNP Id: rs1172554759
MyVariant Identifiers: chr4:g.145522539C>T (hg19) chr4:g.144601387C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601387C>T , CM000666.2:g.144601387C>T GRCh38
NC_000004.11:g.145522539C>T , CM000666.1:g.145522539C>T GRCh37
NC_000004.10:g.145741989C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185409G>A ENSP00000497507.1:n.328-185409G>A
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