Canonical Allele Identifier: CA13035099
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99817185C>G , CM000671.2:g.99817185C>G GRCh38
NC_000009.11:g.102579467C>G , CM000671.1:g.102579467C>G GRCh37
NC_000009.10:g.101619288C>G NCBI36
NG_028910.1:g.331C>G

Transcript Alleles

HGVS Amino-acid Change
NR_109802.1:n.69+2636G>C