Canonical Allele Identifier: CA784579197
Gene:

Linked Data

dbSNP Id: rs1465884192
gnomAD v3: 4-102499912-G-A
gnomAD v4: 4-102499912-G-A
MyVariant Identifiers: chr4:g.103421069G>A (hg19) chr4:g.102499912G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499912G>A , CM000666.2:g.102499912G>A GRCh38
NC_000004.11:g.103421069G>A , CM000666.1:g.103421069G>A GRCh37
NC_000004.10:g.103640101G>A NCBI36
NG_050628.1:g.3584G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1337C>T XP_011530769.1:n.643+1337C>T
NR_136202.1:n.48+2527C>T
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