Canonical Allele Identifier: CA103120434
Gene:

Linked Data

dbSNP Id: rs929093411
gnomAD v3: 4-102501010-C-A
gnomAD v4: 4-102501010-C-A
MyVariant Identifiers: chr4:g.103422167C>A (hg19) chr4:g.102501010C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501010C>A , CM000666.2:g.102501010C>A GRCh38
NC_000004.11:g.103422167C>A , CM000666.1:g.103422167C>A GRCh37
NC_000004.10:g.103641199C>A NCBI36
NG_050628.1:g.4682C>A

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+239G>T XP_011530769.1:n.643+239G>T
NR_136202.1:n.48+1429G>T
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