Canonical Allele Identifier: CA683994837
Gene:

Linked Data

dbSNP Id: rs1446556735

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398658T>C , CM000674.2:g.115398658T>C GRCh38
NC_000012.11:g.115836463T>C , CM000674.1:g.115836463T>C GRCh37
NC_000012.10:g.114320846T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8437A>G
XR_945389.2:n.701+8437A>G