Canonical Allele Identifier: CA2718947627
Gene:

Linked Data

dbSNP Id: rs2117977531
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551061T>G , CM000671.2:g.25551061T>G GRCh38
NC_000009.11:g.25551059T>G , CM000671.1:g.25551059T>G GRCh37
NC_000009.10:g.25541059T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-489A>C
XR_929525.2:n.674-489A>C
Search 100 bp 5'
Search 100 bp 3'