Canonical Allele Identifier: CA2221132813
Gene:

Linked Data

dbSNP Id: rs1961467442

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108640A>C , CM000678.2:g.49108640A>C GRCh38
NC_000016.9:g.49142551A>C , CM000678.1:g.49142551A>C GRCh37
NC_000016.8:g.47700052A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933517.1:n.810+1304T>G
XR_001752138.2:n.591+5336T>G
XR_933517.2:n.810+1304T>G