Canonical Allele Identifier: CA828897335
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1469106071
gnomAD v3: 6-83516698-A-T
gnomAD v4: 6-83516698-A-T
MyVariant Identifiers: chr6:g.84226417A>T (hg19) chr6:g.83516698A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516698A>T , CM000668.2:g.83516698A>T GRCh38
NC_000006.11:g.84226417A>T , CM000668.1:g.84226417A>T GRCh37
NC_000006.10:g.84283136A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369700.4:c.-21+4004A>T MANE Select ENSP00000358714.3:n.-21+4004A>T
ENST00000369700.3:c.-21+4004A>T ENSP00000358714.3:n.-21+4004A>T
NM_001170423.1:c.-126+4004A>T NP_001163894.1:n.-126+4004A>T
NM_153362.2:c.-21+4004A>T NP_699193.2:n.-21+4004A>T
NM_153362.3:c.-21+4004A>T MANE Select NP_699193.2:n.-21+4004A>T
NM_001170423.2:c.-126+4004A>T NP_001163894.1:n.-126+4004A>T
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