Canonical Allele Identifier: CA2493232037
Gene:

Linked Data

dbSNP Id: rs1691633881

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485563T>C , CM000664.2:g.20485563T>C GRCh38
NC_000002.11:g.20685324T>C , CM000664.1:g.20685324T>C GRCh37
NC_000002.10:g.20548805T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_157978.1:n.530+3175A>G