Canonical Allele Identifier: CA141911939
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs979479076
MyVariant Identifiers: chr6:g.84226712T>A (hg19) chr6:g.83516993T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516993T>A , CM000668.2:g.83516993T>A GRCh38
NC_000006.11:g.84226712T>A , CM000668.1:g.84226712T>A GRCh37
NC_000006.10:g.84283431T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+4299T>A MANE Select ENSP00000358714.3:n.-21+4299T>A
ENST00000369700.3:c.-21+4299T>A ENSP00000358714.3:n.-21+4299T>A
NM_001170423.1:c.-126+4299T>A NP_001163894.1:n.-126+4299T>A
NM_153362.2:c.-21+4299T>A NP_699193.2:n.-21+4299T>A
NM_153362.3:c.-21+4299T>A MANE Select NP_699193.2:n.-21+4299T>A
NM_001170423.2:c.-126+4299T>A NP_001163894.1:n.-126+4299T>A
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