Canonical Allele Identifier: CA14420332
Gene:

Linked Data

dbSNP Id: rs10491121
gnomAD v2: 17-34430336-G-A
gnomAD v3: 17-36102943-G-A
gnomAD v4: 17-36102943-G-A
MyVariant Identifiers: chr17:g.34430336G>A (hg19) chr17:g.36102943G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.36102943G>A , CM000679.2:g.36102943G>A GRCh38
NC_000017.10:g.34430336G>A , CM000679.1:g.34430336G>A GRCh37
NC_000017.9:g.31454449G>A NCBI36
NG_033066.2:g.4118G>A

Transcript Alleles

HGVS Amino-acid change
XR_001752866.1:n.1810-4036C>T
Search 100 bp 5'
Search 100 bp 3'