Canonical Allele Identifier: CA440620446
Gene:

Linked Data

gnomAD v4: 4-102501250-T-C
MyVariant Identifiers: chr4:g.103422407T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501250T>C , CM000666.2:g.102501250T>C GRCh38
NC_000004.11:g.103422407T>C , CM000666.1:g.103422407T>C GRCh37
NC_000004.10:g.103641439T>C NCBI36
NG_050628.1:g.4922T>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.642A>G XP_011530769.1:p.Gly214=
NR_136202.1:n.48+1189A>G
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