Canonical Allele Identifier: CA704082180
Gene:

Linked Data

dbSNP Id: rs1450028918
MyVariant Identifiers: chr14:g.21261592C>A (hg19) chr14:g.20793433C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793433C>A , CM000676.2:g.20793433C>A GRCh38
NC_000014.8:g.21261592C>A , CM000676.1:g.21261592C>A GRCh37
NC_000014.7:g.20331432C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+647C>A
XR_943585.1:n.585+647C>A
XR_001750620.1:n.3271+647C>A
XR_001750621.1:n.3271+647C>A
XR_001750622.1:n.637+6471G>T
XR_001750623.1:n.637+6471G>T
XR_001750624.1:n.637+6471G>T
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