Canonical Allele Identifier: CA37327627
Gene:

Linked Data

dbSNP Id: rs149515977
gnomAD v2: 1-213855729-C-T
gnomAD v3: 1-213682386-C-T
gnomAD v4: 1-213682386-C-T
MyVariant Identifiers: chr1:g.213855729C>T (hg19) chr1:g.213682386C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682386C>T , CM000663.2:g.213682386C>T GRCh38
NC_000001.10:g.213855729C>T , CM000663.1:g.213855729C>T GRCh37
NC_000001.9:g.211922352C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49031C>T
XR_001738464.1:n.426-49031C>T
Search 100 bp 5'
Search 100 bp 3'