Canonical Allele Identifier: CA552053303
Gene:

Linked Data

dbSNP Id: rs1383475841
gnomAD v2: 4-63424167-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558449C>G , CM000666.2:g.62558449C>G GRCh38
NC_000004.11:g.63424167C>G , CM000666.1:g.63424167C>G GRCh37
NC_000004.10:g.63106762C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5395C>G