Canonical Allele Identifier: CA402894753

Gene: PRSS57

Linked Data

• dbSNP Id: rs2031748111
• gnomAD v4: 19-694943-C-G
• MyVariant Identifiers: chr19:g.694943C>G (hg19) ; chr19:g.694943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.694943C>G , CM000681.2:g.694943C>G	GRCh38
NC_000019.9:g.694943C>G , CM000681.1:g.694943C>G	GRCh37
NC_000019.8:g.645943C>G	NCBI36
NG_051189.1:g.5589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329267.9:c.104G>C MANE Select	ENSP00000327386.6:p.Gly35Ala
ENST00000329267.8:c.104G>C	ENSP00000327386.6:p.Gly35Ala
ENST00000613411.4:c.107G>C	ENSP00000482358.1:p.Gly36Ala
NM_001308209.1:c.104G>C	NP_001295138.1:p.Gly35Ala
NM_214710.3:c.107G>C	NP_999875.1:p.Gly36Ala
NM_214710.4:c.107G>C	NP_999875.1:p.Gly36Ala
NM_001308209.2:c.104G>C MANE Select	NP_001295138.2:p.Gly35Ala
NM_214710.5:c.107G>C	NP_999875.2:p.Gly36Ala