Canonical Allele Identifier: CA2712203568
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs2127712933
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517165C>T , CM000668.2:g.83517165C>T GRCh38
NC_000006.11:g.84226884C>T , CM000668.1:g.84226884C>T GRCh37
NC_000006.10:g.84283603C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4471C>T MANE Select ENSP00000358714.3:n.-21+4471C>T
ENST00000369700.3:c.-21+4471C>T ENSP00000358714.3:n.-21+4471C>T
NM_001170423.1:c.-125-4370C>T NP_001163894.1:n.-125-4370C>T
NM_153362.2:c.-21+4471C>T NP_699193.2:n.-21+4471C>T
NM_153362.3:c.-21+4471C>T MANE Select NP_699193.2:n.-21+4471C>T
NM_001170423.2:c.-125-4370C>T NP_001163894.1:n.-125-4370C>T
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