Canonical Allele Identifier: CA309668897
Gene:

Linked Data

dbSNP Id: rs560400829
MyVariant Identifiers: chr19:g.51340621C>T (hg19) chr19:g.50837365C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837365C>T , CM000681.2:g.50837365C>T GRCh38
NC_000019.9:g.51340621C>T , CM000681.1:g.51340621C>T GRCh37
NC_000019.8:g.56032433C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6072C>T
NR_131205.1:n.230+6072C>T
XR_936030.1:n.298+6072C>T
XR_936031.1:n.298+6072C>T
XR_936032.1:n.298+6072C>T
XR_936033.1:n.294+6072C>T
XR_936035.1:n.281+6072C>T
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