Canonical Allele Identifier: CA440620406
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422393G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501236G>T , CM000666.2:g.102501236G>T GRCh38
NC_000004.11:g.103422393G>T , CM000666.1:g.103422393G>T GRCh37
NC_000004.10:g.103641425G>T NCBI36
NG_050628.1:g.4908G>T

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+13C>A XP_011530769.1:n.643+13C>A
NR_136202.1:n.48+1203C>A
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