Canonical Allele Identifier: CA1468603699
Gene:

Linked Data

dbSNP Id: rs1750546698
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304424T>A , CM000666.2:g.74304424T>A GRCh38
NC_000004.11:g.75170141T>A , CM000666.1:g.75170141T>A GRCh37
NC_000004.10:g.75389005T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938877.1:n.120-25646A>T
XR_938877.2:n.126-25646A>T
Search 100 bp 5'
Search 100 bp 3'