Canonical Allele Identifier: CA37327630
Gene:

Linked Data

dbSNP Id: rs143146657
gnomAD v2: 1-213855738-T-A
gnomAD v3: 1-213682395-T-A
gnomAD v4: 1-213682395-T-A
MyVariant Identifiers: chr1:g.213855738T>A (hg19) chr1:g.213682395T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682395T>A , CM000663.2:g.213682395T>A GRCh38
NC_000001.10:g.213855738T>A , CM000663.1:g.213855738T>A GRCh37
NC_000001.9:g.211922361T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49022T>A
XR_001738464.1:n.426-49022T>A
Search 100 bp 5'
Search 100 bp 3'