Canonical Allele Identifier: CA12422334

Gene: PRSS35

Linked Data

• dbSNP Id: rs78675001
• gnomAD v2: 6-84226501-G-A
• gnomAD v3: 6-83516782-G-A
• gnomAD v4: 6-83516782-G-A
• MyVariant Identifiers: chr6:g.84226501G>A (hg19) ; chr6:g.83516782G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516782G>A , CM000668.2:g.83516782G>A	GRCh38
NC_000006.11:g.84226501G>A , CM000668.1:g.84226501G>A	GRCh37
NC_000006.10:g.84283220G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369700.4:c.-21+4088G>A MANE Select	ENSP00000358714.3:n.-21+4088G>A
ENST00000369700.3:c.-21+4088G>A	ENSP00000358714.3:n.-21+4088G>A
NM_001170423.1:c.-126+4088G>A	NP_001163894.1:n.-126+4088G>A
NM_153362.2:c.-21+4088G>A	NP_699193.2:n.-21+4088G>A
NM_153362.3:c.-21+4088G>A MANE Select	NP_699193.2:n.-21+4088G>A
NM_001170423.2:c.-126+4088G>A	NP_001163894.1:n.-126+4088G>A