Canonical Allele Identifier: CA440619071
Gene:

Linked Data

gnomAD v4: 4-102500944-C-T
MyVariant Identifiers: chr4:g.103422101C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500944C>T , CM000666.2:g.102500944C>T GRCh38
NC_000004.11:g.103422101C>T , CM000666.1:g.103422101C>T GRCh37
NC_000004.10:g.103641133C>T NCBI36
NG_050628.1:g.4616C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+305G>A XP_011530769.1:n.643+305G>A
NR_136202.1:n.48+1495G>A
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