Canonical Allele Identifier: CA1320446139
Gene:

Linked Data

dbSNP Id: rs2077888884

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033153G>C , CM000664.2:g.200033153G>C GRCh38
NC_000002.11:g.200897876G>C , CM000664.1:g.200897876G>C GRCh37
NC_000002.10:g.200606121G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22257C>G