Canonical Allele Identifier: CA973010742
Gene:

Linked Data

dbSNP Id: rs2076167701
gnomAD v3: 15-94775327-T-C
gnomAD v4: 15-94775327-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.94775327T>C , CM000677.2:g.94775327T>C GRCh38
NC_000015.9:g.95318556T>C , CM000677.1:g.95318556T>C GRCh37
NC_000015.8:g.93119560T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932644.1:n.369-9310A>G
XR_932644.2:n.369-9310A>G
Search 100 bp 5'
Search 100 bp 3'