Canonical Allele Identifier: CA759294401
Gene:

Linked Data

dbSNP Id: rs1416464179
MyVariant Identifiers: chr2:g.156727038T>A (hg19) chr2:g.155870526T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870526T>A , CM000664.2:g.155870526T>A GRCh38
NC_000002.11:g.156727038T>A , CM000664.1:g.156727038T>A GRCh37
NC_000002.10:g.156435284T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3339A>T
XR_001739749.1:n.331-29542A>T
XR_001739750.1:n.331-29542A>T
XR_001739751.1:n.331-29542A>T
XR_923501.2:n.331-3339A>T
Search 100 bp 5'
Search 100 bp 3'