Canonical Allele Identifier: CA76316037
Gene:

Linked Data

dbSNP Id: rs749791384

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61427924G>C , CM000665.2:g.61427924G>C GRCh38
NC_000003.11:g.61413598G>C , CM000665.1:g.61413598G>C GRCh37
NC_000003.10:g.61388638G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.165-238C>G
XR_940893.1:n.164+590C>G
XR_001740725.1:n.202+590C>G
XR_940892.2:n.203-238C>G