Canonical Allele Identifier: CA440619649
Gene:

Linked Data

gnomAD v4: 4-102501011-G-T
MyVariant Identifiers: chr4:g.103422168G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501011G>T , CM000666.2:g.102501011G>T GRCh38
NC_000004.11:g.103422168G>T , CM000666.1:g.103422168G>T GRCh37
NC_000004.10:g.103641200G>T NCBI36
NG_050628.1:g.4683G>T

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+238C>A XP_011530769.1:n.643+238C>A
NR_136202.1:n.48+1428C>A
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