Canonical Allele Identifier: CA1841175606
Gene:

Linked Data

dbSNP Id: rs748979721

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551469C>G , CM000671.2:g.25551469C>G GRCh38
NC_000009.11:g.25551467C>G , CM000671.1:g.25551467C>G GRCh37
NC_000009.10:g.25541467C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-897G>C
XR_929525.2:n.674-897G>C