Canonical Allele Identifier: CA1104780650
Gene:

Linked Data

dbSNP Id: rs1789258459
gnomAD v3: 7-97388598-G-T
gnomAD v4: 7-97388598-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388598G>T , CM000669.2:g.97388598G>T GRCh38
NC_000007.13:g.97017910G>T , CM000669.1:g.97017910G>T GRCh37
NC_000007.12:g.96855846G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59951C>A