Canonical Allele Identifier: CA440618947
Gene:

Linked Data

gnomAD v4: 4-102500912-G-T
MyVariant Identifiers: chr4:g.103422069G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500912G>T , CM000666.2:g.102500912G>T GRCh38
NC_000004.11:g.103422069G>T , CM000666.1:g.103422069G>T GRCh37
NC_000004.10:g.103641101G>T NCBI36
NG_050628.1:g.4584G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+337C>A XP_011530769.1:n.643+337C>A
NR_136202.1:n.48+1527C>A
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