Canonical Allele Identifier: CA568294612
Gene: PRSS35 HGNC NCBI

Linked Data

dbSNP Id: rs1301932756
gnomAD v2: 6-84226876-A-G
gnomAD v3: 6-83517157-A-G
gnomAD v4: 6-83517157-A-G
MyVariant Identifiers: chr6:g.84226876A>G (hg19) chr6:g.83517157A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83517157A>G , CM000668.2:g.83517157A>G GRCh38
NC_000006.11:g.84226876A>G , CM000668.1:g.84226876A>G GRCh37
NC_000006.10:g.84283595A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369700.4:c.-21+4463A>G MANE Select ENSP00000358714.3:n.-21+4463A>G
ENST00000369700.3:c.-21+4463A>G ENSP00000358714.3:n.-21+4463A>G
NM_001170423.1:c.-125-4378A>G NP_001163894.1:n.-125-4378A>G
NM_153362.2:c.-21+4463A>G NP_699193.2:n.-21+4463A>G
NM_153362.3:c.-21+4463A>G MANE Select NP_699193.2:n.-21+4463A>G
NM_001170423.2:c.-125-4378A>G NP_001163894.1:n.-125-4378A>G
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