Canonical Allele Identifier: CA12199167
Gene: PRSS35 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1171113

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516876C>T , CM000668.2:g.83516876C>T GRCh38
NC_000006.11:g.84226595C>T , CM000668.1:g.84226595C>T GRCh37
NC_000006.10:g.84283314C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001170423.1:c.-126+4182C>T VV NP_001163894.1:p.=
NM_153362.2:c.-21+4182C>T VV NP_699193.2:p.=
NM_153362.3:c.-21+4182C>T VV MANE Preferred
ENST00000369700.3:c.-21+4182C>T ENSP00000358714.3:p.=