Canonical Allele Identifier: CA568294596
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1459941968
gnomAD v2: 6-84226545-G-T
gnomAD v3: 6-83516826-G-T
gnomAD v4: 6-83516826-G-T
MyVariant Identifiers: chr6:g.84226545G>T (hg19) chr6:g.83516826G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516826G>T , CM000668.2:g.83516826G>T GRCh38
NC_000006.11:g.84226545G>T , CM000668.1:g.84226545G>T GRCh37
NC_000006.10:g.84283264G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4132G>T MANE Select ENSP00000358714.3:n.-21+4132G>T
ENST00000369700.3:c.-21+4132G>T ENSP00000358714.3:n.-21+4132G>T
NM_001170423.1:c.-126+4132G>T NP_001163894.1:n.-126+4132G>T
NM_153362.2:c.-21+4132G>T NP_699193.2:n.-21+4132G>T
NM_153362.3:c.-21+4132G>T MANE Select NP_699193.2:n.-21+4132G>T
NM_001170423.2:c.-126+4132G>T NP_001163894.1:n.-126+4132G>T
Search 100 bp 5'
Search 100 bp 3'