Canonical Allele Identifier: CA20757612
Gene:

Linked Data

dbSNP Id: rs763706247
gnomAD v2: 1-34989174-T-C
gnomAD v3: 1-34523573-T-C
gnomAD v4: 1-34523573-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523573T>C , CM000663.2:g.34523573T>C GRCh38
NC_000001.10:g.34989174T>C , CM000663.1:g.34989174T>C GRCh37
NC_000001.9:g.34761761T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+24006A>G
XR_001737964.1:n.991+24006A>G