Canonical Allele Identifier: CA1858359262
Gene:

Linked Data

dbSNP Id: rs2076503464

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.79731013T>G , CM000671.2:g.79731013T>G GRCh38
NC_000009.11:g.82345928T>G , CM000671.1:g.82345928T>G GRCh37
NC_000009.10:g.81535748T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929980.1:n.1019+701T>G