Canonical Allele Identifier: CA2642457437
Gene:

Linked Data

gnomAD v4: 1-817312-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.817312T>C , CM000663.2:g.817312T>C GRCh38
NC_000001.10:g.752692T>C , CM000663.1:g.752692T>C GRCh37
NC_000001.9:g.742555T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000634337.2:n.127+10358A>G
ENST00000635509.2:n.100+10358A>G
ENST00000447500.4:n.340+61A>G