Canonical Allele Identifier: CA1500738999
Gene:

Linked Data

dbSNP Id: rs1727412584
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601372C>A , CM000666.2:g.144601372C>A GRCh38
NC_000004.11:g.145522524C>A , CM000666.1:g.145522524C>A GRCh37
NC_000004.10:g.145741974C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185394G>T ENSP00000497507.1:n.328-185394G>T
Search 100 bp 5'
Search 100 bp 3'