Canonical Allele Identifier: CA619725781
Gene:

Linked Data

dbSNP Id: rs1402444261
gnomAD v2: 15-87695380-T-C
gnomAD v3: 15-87152149-T-C
gnomAD v4: 15-87152149-T-C
MyVariant Identifiers: chr15:g.87695380T>C (hg19) chr15:g.87152149T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152149T>C , CM000677.2:g.87152149T>C GRCh38
NC_000015.9:g.87695380T>C , CM000677.1:g.87695380T>C GRCh37
NC_000015.8:g.85496384T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26078T>C
XR_932582.2:n.167-26078T>C
Search 100 bp 5'
Search 100 bp 3'