Canonical Allele Identifier: CA798354173
Gene:

Linked Data

dbSNP Id: rs1441571199
MyVariant Identifiers: chr4:g.75170103A>G (hg19) chr4:g.74304386A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304386A>G , CM000666.2:g.74304386A>G GRCh38
NC_000004.11:g.75170103A>G , CM000666.1:g.75170103A>G GRCh37
NC_000004.10:g.75388967A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938877.1:n.120-25608T>C
XR_938877.2:n.126-25608T>C
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