Canonical Allele Identifier: CA568294579
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1174054707
gnomAD v2: 6-84226309-A-C
gnomAD v3: 6-83516590-A-C
gnomAD v4: 6-83516590-A-C
MyVariant Identifiers: chr6:g.84226309A>C (hg19) chr6:g.83516590A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83516590A>C , CM000668.2:g.83516590A>C GRCh38
NC_000006.11:g.84226309A>C , CM000668.1:g.84226309A>C GRCh37
NC_000006.10:g.84283028A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+3896A>C MANE Select ENSP00000358714.3:n.-21+3896A>C
ENST00000369700.3:c.-21+3896A>C ENSP00000358714.3:n.-21+3896A>C
NM_001170423.1:c.-126+3896A>C NP_001163894.1:n.-126+3896A>C
NM_153362.2:c.-21+3896A>C NP_699193.2:n.-21+3896A>C
NM_153362.3:c.-21+3896A>C MANE Select NP_699193.2:n.-21+3896A>C
NM_001170423.2:c.-126+3896A>C NP_001163894.1:n.-126+3896A>C
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