Canonical Allele Identifier: CA1252497446
Gene:

Linked Data

dbSNP Id: rs1367226

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.55862405A>C , CM000664.2:g.55862405A>C GRCh38
NC_000002.11:g.56089540A>C , CM000664.1:g.56089540A>C GRCh37
NC_000002.10:g.55943044A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940108.1:n.229-11478A>C
XR_002959388.1:n.229-11478A>C