Canonical Allele Identifier: CA1468603719
Gene:

Linked Data

dbSNP Id: rs1750547746
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304468A>T , CM000666.2:g.74304468A>T GRCh38
NC_000004.11:g.75170185A>T , CM000666.1:g.75170185A>T GRCh37
NC_000004.10:g.75389049A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938877.1:n.120-25690T>A
XR_938877.2:n.126-25690T>A
Search 100 bp 5'
Search 100 bp 3'