Canonical Allele Identifier: CA440619604
Gene:

Linked Data

gnomAD v4: 4-102500998-A-C
MyVariant Identifiers: chr4:g.103422155A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500998A>C , CM000666.2:g.102500998A>C GRCh38
NC_000004.11:g.103422155A>C , CM000666.1:g.103422155A>C GRCh37
NC_000004.10:g.103641187A>C NCBI36
NG_050628.1:g.4670A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+251T>G XP_011530769.1:n.643+251T>G
NR_136202.1:n.48+1441T>G
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