Canonical Allele Identifier: CA527707461
Gene:

Linked Data

dbSNP Id: rs10737621
gnomAD v2: 1-193090865-C-T
gnomAD v3: 1-193121735-C-T
gnomAD v4: 1-193121735-C-T
MyVariant Identifiers: chr1:g.193090865C>T (hg19) chr1:g.193121735C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121735C>T , CM000663.2:g.193121735C>T GRCh38
NC_000001.10:g.193090865C>T , CM000663.1:g.193090865C>T GRCh37
NC_000001.9:g.191357488C>T NCBI36
NG_012691.1:g.4778C>T , LRG_507:g.4778C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1922G>A
Search 100 bp 5'
Search 100 bp 3'