Canonical Allele Identifier: CA103120298
Gene:

Linked Data

dbSNP Id: rs753526281
gnomAD v3: 4-102500043-C-G
gnomAD v4: 4-102500043-C-G
MyVariant Identifiers: chr4:g.103421200C>G (hg19) chr4:g.102500043C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500043C>G , CM000666.2:g.102500043C>G GRCh38
NC_000004.11:g.103421200C>G , CM000666.1:g.103421200C>G GRCh37
NC_000004.10:g.103640232C>G NCBI36
NG_050628.1:g.3715C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1206G>C XP_011530769.1:n.643+1206G>C
NR_136202.1:n.48+2396G>C
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