Canonical Allele Identifier: CA568294592

Gene: PRSS35

Linked Data

• dbSNP Id: rs1290394321
• gnomAD v2: 6-84226515-C-G
• gnomAD v3: 6-83516796-C-G
• gnomAD v4: 6-83516796-C-G
• MyVariant Identifiers: chr6:g.84226515C>G (hg19) ; chr6:g.83516796C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516796C>G , CM000668.2:g.83516796C>G	GRCh38
NC_000006.11:g.84226515C>G , CM000668.1:g.84226515C>G	GRCh37
NC_000006.10:g.84283234C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369700.4:c.-21+4102C>G MANE Select	ENSP00000358714.3:n.-21+4102C>G
ENST00000369700.3:c.-21+4102C>G	ENSP00000358714.3:n.-21+4102C>G
NM_001170423.1:c.-126+4102C>G	NP_001163894.1:n.-126+4102C>G
NM_153362.2:c.-21+4102C>G	NP_699193.2:n.-21+4102C>G
NM_153362.3:c.-21+4102C>G MANE Select	NP_699193.2:n.-21+4102C>G
NM_001170423.2:c.-126+4102C>G	NP_001163894.1:n.-126+4102C>G