Canonical Allele Identifier: CA537204322
Gene:

Linked Data

dbSNP Id: rs1393750306
gnomAD v2: 2-156726713-T-A
gnomAD v3: 2-155870201-T-A
gnomAD v4: 2-155870201-T-A
MyVariant Identifiers: chr2:g.156726713T>A (hg19) chr2:g.155870201T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870201T>A , CM000664.2:g.155870201T>A GRCh38
NC_000002.11:g.156726713T>A , CM000664.1:g.156726713T>A GRCh37
NC_000002.10:g.156434959T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3014A>T
XR_001739749.1:n.331-29217A>T
XR_001739750.1:n.331-29217A>T
XR_001739751.1:n.331-29217A>T
XR_923501.2:n.331-3014A>T
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