Canonical Allele Identifier: CA11146286
Gene:

Linked Data

dbSNP Id: rs1568282
gnomAD v2: 2-15066177-C-T
gnomAD v3: 2-14926053-C-T
gnomAD v4: 2-14926053-C-T
MyVariant Identifiers: chr2:g.15066177C>T (hg19) chr2:g.14926053C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.14926053C>T , CM000664.2:g.14926053C>T GRCh38
NC_000002.11:g.15066177C>T , CM000664.1:g.15066177C>T GRCh37
NC_000002.10:g.14983628C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922818.1:n.205-146906G>A
Search 100 bp 5'
Search 100 bp 3'