Canonical Allele Identifier: CA1869965246
Gene:

Linked Data

dbSNP Id: rs1826506592

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928267G>C , CM000671.2:g.104928267G>C GRCh38
NC_000009.11:g.107690548G>C , CM000671.1:g.107690548G>C GRCh37
NC_000009.10:g.106730369G>C NCBI36
NG_007981.1:g.4889C>G

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+357G>C
XR_930204.2:n.115+357G>C