Canonical Allele Identifier: CA141911787
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs554969239
gnomAD v2: 6-84226408-T-C
gnomAD v3: 6-83516689-T-C
gnomAD v4: 6-83516689-T-C
MyVariant Identifiers: chr6:g.84226408T>C (hg19) chr6:g.83516689T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516689T>C , CM000668.2:g.83516689T>C GRCh38
NC_000006.11:g.84226408T>C , CM000668.1:g.84226408T>C GRCh37
NC_000006.10:g.84283127T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+3995T>C MANE Select ENSP00000358714.3:n.-21+3995T>C
ENST00000369700.3:c.-21+3995T>C ENSP00000358714.3:n.-21+3995T>C
NM_001170423.1:c.-126+3995T>C NP_001163894.1:n.-126+3995T>C
NM_153362.2:c.-21+3995T>C NP_699193.2:n.-21+3995T>C
NM_153362.3:c.-21+3995T>C MANE Select NP_699193.2:n.-21+3995T>C
NM_001170423.2:c.-126+3995T>C NP_001163894.1:n.-126+3995T>C
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