Canonical Allele Identifier: CA337768404
Gene:

Linked Data

dbSNP Id: rs1016505967

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15311455C>A , CM000686.2:g.15311455C>A GRCh38
NC_000024.9:g.17423335C>A , CM000686.1:g.17423335C>A GRCh37
NC_000024.8:g.15932729C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001756089.1:n.309+37214G>T