Canonical Allele Identifier: CA440620463
Gene:

Linked Data

gnomAD v4: 4-102501256-C-T
MyVariant Identifiers: chr4:g.103422413C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501256C>T , CM000666.2:g.102501256C>T GRCh38
NC_000004.11:g.103422413C>T , CM000666.1:g.103422413C>T GRCh37
NC_000004.10:g.103641445C>T NCBI36
NG_050628.1:g.4928C>T

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.636G>A XP_011530769.1:p.Gly212=
NR_136202.1:n.48+1183G>A
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