Canonical Allele Identifier: CA1332325170
Gene:

Linked Data

dbSNP Id: rs1691990875

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.226155973C>T , CM000664.2:g.226155973C>T GRCh38
NC_000002.11:g.227020689C>T , CM000664.1:g.227020689C>T GRCh37
NC_000002.10:g.226728933C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046102.1:n.293-8415C>T