Canonical Allele Identifier: CA537204547
Gene:

Linked Data

dbSNP Id: rs367717234
gnomAD v2: 2-156727189-C-A
gnomAD v3: 2-155870677-C-A
gnomAD v4: 2-155870677-C-A
MyVariant Identifiers: chr2:g.156727189C>A (hg19) chr2:g.155870677C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870677C>A , CM000664.2:g.155870677C>A GRCh38
NC_000002.11:g.156727189C>A , CM000664.1:g.156727189C>A GRCh37
NC_000002.10:g.156435435C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3490G>T
XR_001739749.1:n.331-29693G>T
XR_001739750.1:n.331-29693G>T
XR_001739751.1:n.331-29693G>T
XR_923501.2:n.331-3490G>T
Search 100 bp 5'
Search 100 bp 3'