Canonical Allele Identifier: CA904086781
Gene:

Linked Data

dbSNP Id: rs1241677508
MyVariant Identifiers: chr3:g.187649462C>T (hg19) chr3:g.187931674C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931674C>T , CM000665.2:g.187931674C>T GRCh38
NC_000003.11:g.187649462C>T , CM000665.1:g.187649462C>T GRCh37
NC_000003.10:g.189132156C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1240G>A
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