Canonical Allele Identifier: CA59107037
Gene:

Linked Data

dbSNP Id: rs997895552
gnomAD v2: 2-156726673-G-A
gnomAD v3: 2-155870161-G-A
gnomAD v4: 2-155870161-G-A
MyVariant Identifiers: chr2:g.156726673G>A (hg19) chr2:g.155870161G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870161G>A , CM000664.2:g.155870161G>A GRCh38
NC_000002.11:g.156726673G>A , CM000664.1:g.156726673G>A GRCh37
NC_000002.10:g.156434919G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-2974C>T
XR_001739749.1:n.331-29177C>T
XR_001739750.1:n.331-29177C>T
XR_001739751.1:n.331-29177C>T
XR_923501.2:n.331-2974C>T
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