Canonical Allele Identifier: CA168173036

Gene: PRSS2 TRBC1

Linked Data

• dbSNP Id: rs373862862
• gnomAD v2: 7-142482061-C-G
• gnomAD v3: 7-142774201-C-G
• gnomAD v4: 7-142774201-C-G
• MyVariant Identifiers: chr7:g.142482061C>G (hg19) ; chr7:g.142774201C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142774201C>G , CM000669.2:g.142774201C>G	GRCh38
NC_000007.13:g.142482061C>G , CM000669.1:g.142482061C>G	GRCh37
NC_000007.12:g.142182004C>G	NCBI36
NG_008322.2:g.8259C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539842.6:c.591+146C>G (PRSS2) MANE Select	ENSP00000488338.1:n.591+146C>G
ENST00000539842.5:c.591+146C>G (PRSS2)	ENSP00000488338.1:n.591+146C>G
ENST00000610416.2:c.371-12837C>G (TRBC1)	ENSP00000482915.1:n.371-12837C>G
ENST00000618750.2:n.425-155C>G (PRSS2)
ENST00000632805.1:c.588+146C>G (PRSS2)	ENSP00000488077.1:n.588+146C>G
ENST00000632998.1:c.591+146C>G (PRSS2)	ENSP00000488789.1:n.591+146C>G
ENST00000633114.1:c.597+146C>G (PRSS2)	ENSP00000487822.1:n.597+146C>G
ENST00000633969.1:c.633+146C>G (PRSS2)	ENSP00000488437.1:n.633+146C>G
ENST00000634019.1:c.633+146C>G (PRSS2)	ENSP00000488594.1:n.633+146C>G
NM_001303414.1:c.633+146C>G (PRSS2)	NP_001290343.1:n.633+146C>G
NM_002770.3:c.591+146C>G (PRSS2)	NP_002761.1:n.591+146C>G
NR_130149.1:n.557+146C>G (PRSS2)
NM_002770.4:c.591+146C>G (PRSS2) MANE Select	NP_002761.1:n.591+146C>G
NR_130149.2:n.530+146C>G (PRSS2)
NM_001303414.2:c.633+146C>G (PRSS2)	NP_001290343.1:n.633+146C>G