Canonical Allele Identifier: CA59107040
Gene:

Linked Data

dbSNP Id: rs953606364
gnomAD v3: 2-155870191-G-A
gnomAD v4: 2-155870191-G-A
MyVariant Identifiers: chr2:g.156726703G>A (hg19) chr2:g.155870191G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870191G>A , CM000664.2:g.155870191G>A GRCh38
NC_000002.11:g.156726703G>A , CM000664.1:g.156726703G>A GRCh37
NC_000002.10:g.156434949G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3004C>T
XR_001739749.1:n.331-29207C>T
XR_001739750.1:n.331-29207C>T
XR_001739751.1:n.331-29207C>T
XR_923501.2:n.331-3004C>T
Search 100 bp 5'
Search 100 bp 3'