Canonical Allele Identifier: CA440618902
Gene:

Linked Data

dbSNP Id: rs1156630026
gnomAD v3: 4-102500903-G-A
gnomAD v4: 4-102500903-G-A
MyVariant Identifiers: chr4:g.103422060G>A (hg19) chr4:g.102500903G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500903G>A , CM000666.2:g.102500903G>A GRCh38
NC_000004.11:g.103422060G>A , CM000666.1:g.103422060G>A GRCh37
NC_000004.10:g.103641092G>A NCBI36
NG_050628.1:g.4575G>A

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+346C>T XP_011530769.1:n.643+346C>T
NR_136202.1:n.48+1536C>T
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