Canonical Allele Identifier: CA786695493
Gene:

Linked Data

dbSNP Id: rs1470169913
MyVariant Identifiers: chr4:g.12579637A>T (hg19) chr4:g.12578013A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578013A>T , CM000666.2:g.12578013A>T GRCh38
NC_000004.11:g.12579637A>T , CM000666.1:g.12579637A>T GRCh37
NC_000004.10:g.12188735A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31329T>A
XR_001741374.1:n.254+44642T>A
XR_925406.3:n.140+31329T>A
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