Canonical Allele Identifier: CA440620307
Gene:

Linked Data

dbSNP Id: rs1738979638
MyVariant Identifiers: chr4:g.103422359G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501202G>C , CM000666.2:g.102501202G>C GRCh38
NC_000004.11:g.103422359G>C , CM000666.1:g.103422359G>C GRCh37
NC_000004.10:g.103641391G>C NCBI36
NG_050628.1:g.4874G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+47C>G XP_011530769.1:n.643+47C>G
NR_136202.1:n.48+1237C>G
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