Canonical Allele Identifier: CA280996497
Gene:

Linked Data

dbSNP Id: rs1012986339
MyVariant Identifiers: chr16:g.49142771G>T (hg19) chr16:g.49108860G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108860G>T , CM000678.2:g.49108860G>T GRCh38
NC_000016.9:g.49142771G>T , CM000678.1:g.49142771G>T GRCh37
NC_000016.8:g.47700272G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1084C>A
XR_001752138.2:n.591+5116C>A
XR_933517.2:n.810+1084C>A
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