Canonical Allele Identifier: CA271499825
Gene: FAM81A HGNC NCBI

Linked Data

dbSNP Id: rs576689398
gnomAD v3: 15-59419542-T-C
gnomAD v4: 15-59419542-T-C
MyVariant Identifiers: chr15:g.59711741T>C (hg19) chr15:g.59419542T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419542T>C , CM000677.2:g.59419542T>C GRCh38
NC_000015.9:g.59711741T>C , CM000677.1:g.59711741T>C GRCh37
NC_000015.8:g.57499033T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17184T>C ENSP00000453918.1:n.-78+17184T>C
ENST00000560394.5:c.-78+17184T>C ENSP00000452962.1:n.-78+17184T>C
XM_006720399.1:c.-78+17184T>C XP_006720462.1:n.-78+17184T>C
XM_011521248.1:c.-22+17184T>C XP_011519550.1:n.-22+17184T>C
XM_011521248.2:c.-22+17184T>C XP_011519550.1:n.-22+17184T>C
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