Canonical Allele Identifier: CA578625953

Gene: PRSS2 TRBC1

Linked Data

• dbSNP Id: rs1554507195
• gnomAD v2: 7-142482085-A-T
• MyVariant Identifiers: chr7:g.142482085A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142774225A>T , CM000669.2:g.142774225A>T	GRCh38
NC_000007.13:g.142482085A>T , CM000669.1:g.142482085A>T	GRCh37
NC_000007.12:g.142182028A>T	NCBI36
NG_008322.2:g.8283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539842.6:c.592-131A>T (PRSS2) MANE Select	ENSP00000488338.1:n.592-131A>T
ENST00000539842.5:c.592-131A>T (PRSS2)	ENSP00000488338.1:n.592-131A>T
ENST00000610416.2:c.371-12813A>T (TRBC1)	ENSP00000482915.1:n.371-12813A>T
ENST00000618750.2:n.425-131A>T (PRSS2)
ENST00000632805.1:c.589-131A>T (PRSS2)	ENSP00000488077.1:n.589-131A>T
ENST00000632998.1:c.592-131A>T (PRSS2)	ENSP00000488789.1:n.592-131A>T
ENST00000633114.1:c.598-131A>T (PRSS2)	ENSP00000487822.1:n.598-131A>T
ENST00000633969.1:c.634-131A>T (PRSS2)	ENSP00000488437.1:n.634-131A>T
ENST00000634019.1:c.634-131A>T (PRSS2)	ENSP00000488594.1:n.634-131A>T
NM_001303414.1:c.634-131A>T (PRSS2)	NP_001290343.1:n.634-131A>T
NM_002770.3:c.592-131A>T (PRSS2)	NP_002761.1:n.592-131A>T
NR_130149.1:n.558-131A>T (PRSS2)
NM_002770.4:c.592-131A>T (PRSS2) MANE Select	NP_002761.1:n.592-131A>T
NR_130149.2:n.531-131A>T (PRSS2)
NM_001303414.2:c.634-131A>T (PRSS2)	NP_001290343.1:n.634-131A>T