Canonical Allele Identifier: CA883240770
Gene:

Linked Data

dbSNP Id: rs1199295744
MyVariant Identifiers: chr19:g.51341140T>C (hg19) chr19:g.50837884T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837884T>C , CM000681.2:g.50837884T>C GRCh38
NC_000019.9:g.51341140T>C , CM000681.1:g.51341140T>C GRCh37
NC_000019.8:g.56032952T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6591T>C
NR_131205.1:n.230+6591T>C
XR_936030.1:n.298+6591T>C
XR_936031.1:n.298+6591T>C
XR_936032.1:n.298+6591T>C
XR_936033.1:n.294+6591T>C
XR_936035.1:n.281+6591T>C
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