Canonical Allele Identifier: CA1735257890
Gene:

Linked Data

dbSNP Id: rs1793101241

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.112988321G>T , CM000669.2:g.112988321G>T GRCh38
NC_000007.13:g.112628376G>T , CM000669.1:g.112628376G>T GRCh37
NC_000007.12:g.112415612G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110162.1:n.77-1657C>A