Canonical Allele Identifier: CA2491383677
Gene:

Linked Data

dbSNP Id: rs1664553950

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458330G>A , CM000664.2:g.16458330G>A GRCh38
NC_000002.11:g.16639598G>A , CM000664.1:g.16639598G>A GRCh37
NC_000002.10:g.16503079G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3236C>T