Canonical Allele Identifier: CA440620452
Gene:

Linked Data

dbSNP Id: rs1195243673
MyVariant Identifiers: chr4:g.103422409C>G (hg19) chr4:g.102501252C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501252C>G , CM000666.2:g.102501252C>G GRCh38
NC_000004.11:g.103422409C>G , CM000666.1:g.103422409C>G GRCh37
NC_000004.10:g.103641441C>G NCBI36
NG_050628.1:g.4924C>G

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.640G>C XP_011530769.1:p.Gly214Arg
NR_136202.1:n.48+1187G>C
Search 100 bp 5'
Search 100 bp 3'