Canonical Allele Identifier: CA784579204
Gene:

Linked Data

dbSNP Id: rs1316628916
MyVariant Identifiers: chr4:g.103421115A>G (hg19) chr4:g.102499958A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499958A>G , CM000666.2:g.102499958A>G GRCh38
NC_000004.11:g.103421115A>G , CM000666.1:g.103421115A>G GRCh37
NC_000004.10:g.103640147A>G NCBI36
NG_050628.1:g.3630A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1291T>C XP_011530769.1:n.643+1291T>C
NR_136202.1:n.48+2481T>C
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