Canonical Allele Identifier: CA527707486
Gene:

Linked Data

dbSNP Id: rs1254461535
gnomAD v2: 1-193090920-C-T
gnomAD v3: 1-193121790-C-T
gnomAD v4: 1-193121790-C-T
MyVariant Identifiers: chr1:g.193090920C>T (hg19) chr1:g.193121790C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121790C>T , CM000663.2:g.193121790C>T GRCh38
NC_000001.10:g.193090920C>T , CM000663.1:g.193090920C>T GRCh37
NC_000001.9:g.191357543C>T NCBI36
NG_012691.1:g.4833C>T , LRG_507:g.4833C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1867G>A
Search 100 bp 5'
Search 100 bp 3'