Canonical Allele Identifier: CA15134693
Gene:

Linked Data

dbSNP Id: rs6694400
gnomAD v2: 1-225074736-T-A
gnomAD v3: 1-224887034-T-A
gnomAD v4: 1-224887034-T-A
MyVariant Identifiers: chr1:g.225074736T>A (hg19) chr1:g.224887034T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887034T>A , CM000663.2:g.224887034T>A GRCh38
NC_000001.10:g.225074736T>A , CM000663.1:g.225074736T>A GRCh37
NC_000001.9:g.223141359T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2253A>T
XR_949207.2:n.63-2253A>T
Search 100 bp 5'
Search 100 bp 3'