Canonical Allele Identifier: CA786695458
Gene:

Linked Data

dbSNP Id: rs1447694956
MyVariant Identifiers: chr4:g.12579480C>G (hg19) chr4:g.12577856C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12577856C>G , CM000666.2:g.12577856C>G GRCh38
NC_000004.11:g.12579480C>G , CM000666.1:g.12579480C>G GRCh37
NC_000004.10:g.12188578C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31486G>C
XR_001741374.1:n.254+44799G>C
XR_925406.3:n.140+31486G>C
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