Canonical Allele Identifier: CA2492005204
Gene:

Linked Data

dbSNP Id: rs1673969676

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844024C>T , CM000664.2:g.17844024C>T GRCh38
NC_000002.11:g.18025291C>T , CM000664.1:g.18025291C>T GRCh37
NC_000002.10:g.17888772C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3670G>A