Canonical Allele Identifier: CA2699049847
Gene:

Linked Data

dbSNP Id: rs2149254482

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485733G>C , CM000664.2:g.20485733G>C GRCh38
NC_000002.11:g.20685494G>C , CM000664.1:g.20685494G>C GRCh37
NC_000002.10:g.20548975G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_157978.1:n.530+3005C>G