Canonical Allele Identifier: CA141911828

Gene: PRSS35

Linked Data

• dbSNP Id: rs767611068
• gnomAD v2: 6-84226498-C-T
• gnomAD v3: 6-83516779-C-T
• gnomAD v4: 6-83516779-C-T
• MyVariant Identifiers: chr6:g.84226498C>T (hg19) ; chr6:g.83516779C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83516779C>T , CM000668.2:g.83516779C>T	GRCh38
NC_000006.11:g.84226498C>T , CM000668.1:g.84226498C>T	GRCh37
NC_000006.10:g.84283217C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369700.4:c.-21+4085C>T MANE Select	ENSP00000358714.3:n.-21+4085C>T
ENST00000369700.3:c.-21+4085C>T	ENSP00000358714.3:n.-21+4085C>T
NM_001170423.1:c.-126+4085C>T	NP_001163894.1:n.-126+4085C>T
NM_153362.2:c.-21+4085C>T	NP_699193.2:n.-21+4085C>T
NM_153362.3:c.-21+4085C>T MANE Select	NP_699193.2:n.-21+4085C>T
NM_001170423.2:c.-126+4085C>T	NP_001163894.1:n.-126+4085C>T