Canonical Allele Identifier: CA735235314
Gene:

Linked Data

dbSNP Id: rs1307334639
gnomAD v3: 1-34523575-T-C
gnomAD v4: 1-34523575-T-C
MyVariant Identifiers: chr1:g.34989176T>C (hg19) chr1:g.34523575T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523575T>C , CM000663.2:g.34523575T>C GRCh38
NC_000001.10:g.34989176T>C , CM000663.1:g.34989176T>C GRCh37
NC_000001.9:g.34761763T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+24004A>G
XR_001737964.1:n.991+24004A>G
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