Canonical Allele Identifier: CA440620437
Gene:

Linked Data

gnomAD v4: 4-102501247-A-G
MyVariant Identifiers: chr4:g.103422404A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501247A>G , CM000666.2:g.102501247A>G GRCh38
NC_000004.11:g.103422404A>G , CM000666.1:g.103422404A>G GRCh37
NC_000004.10:g.103641436A>G NCBI36
NG_050628.1:g.4919A>G

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+2T>C XP_011530769.1:n.643+2T>C
NR_136202.1:n.48+1192T>C
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