Canonical Allele Identifier: CA1009193389
Gene:

Linked Data

dbSNP Id: rs1660425008
gnomAD v3: 1-172741771-T-C
gnomAD v4: 1-172741771-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741771T>C , CM000663.2:g.172741771T>C GRCh38
NC_000001.10:g.172710911T>C , CM000663.1:g.172710911T>C GRCh37
NC_000001.9:g.170977534T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922289.1:n.27-34048T>C
Search 100 bp 5'
Search 100 bp 3'