Canonical Allele Identifier: CA1009193454
Gene:

Linked Data

dbSNP Id: rs1660426806
gnomAD v3: 1-172741902-T-C
gnomAD v4: 1-172741902-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741902T>C , CM000663.2:g.172741902T>C GRCh38
NC_000001.10:g.172711042T>C , CM000663.1:g.172711042T>C GRCh37
NC_000001.9:g.170977665T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33917T>C
Search 100 bp 5'
Search 100 bp 3'