Canonical Allele Identifier: CA103120238
Gene:

Linked Data

dbSNP Id: rs1022173880
MyVariant Identifiers: chr4:g.103420764C>G (hg19) chr4:g.102499607C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499607C>G , CM000666.2:g.102499607C>G GRCh38
NC_000004.11:g.103420764C>G , CM000666.1:g.103420764C>G GRCh37
NC_000004.10:g.103639796C>G NCBI36
NG_050628.1:g.3279C>G

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1642G>C XP_011530769.1:n.643+1642G>C
NR_136202.1:n.48+2832G>C
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