Canonical Allele Identifier: CA54965478
Gene:

Linked Data

dbSNP Id: rs772604815

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368913A>C , CM000664.2:g.122368913A>C GRCh38
NC_000002.11:g.123126489A>C , CM000664.1:g.123126489A>C GRCh37
NC_000002.10:g.122842959A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24050A>C
XR_001739684.1:n.556-24050A>C