Canonical Allele Identifier: CA595318359
Gene:

Linked Data

dbSNP Id: rs935243151
gnomAD v2: 10-96522353-G-T
gnomAD v3: 10-94762596-G-T
gnomAD v4: 10-94762596-G-T
MyVariant Identifiers: chr10:g.96522353G>T (hg19) chr10:g.94762596G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762596G>T , CM000672.2:g.94762596G>T GRCh38
NC_000010.10:g.96522353G>T , CM000672.1:g.96522353G>T GRCh37
NC_000010.9:g.96512343G>T NCBI36
NG_008384.2:g.4891G>T
NG_008384.3:g.4916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12462G>T ENSP00000483243.1:n.932-12462G>T
Search 100 bp 5'
Search 100 bp 3'