Canonical Allele Identifier: CA13828796
Gene:

Linked Data

dbSNP Id: rs1207568
gnomAD v2: 13-33590184-G-A
gnomAD v3: 13-33016046-G-A
gnomAD v4: 13-33016046-G-A
MyVariant Identifiers: chr13:g.33590184G>A (hg19) chr13:g.33016046G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33016046G>A , CM000675.2:g.33016046G>A GRCh38
NC_000013.10:g.33590184G>A , CM000675.1:g.33590184G>A GRCh37
NC_000013.9:g.32488184G>A NCBI36
NG_011485.1:g.4614G>A

Transcript Alleles

HGVS Amino-acid change
XM_011535348.1:c.292C>T XP_011533650.1:p.Pro98Ser
Search 100 bp 5'
Search 100 bp 3'