Canonical Allele Identifier: CA449982152

Gene: PI16

Linked Data

• dbSNP Id: rs1763165051
• gnomAD v4: 6-36954919-C-T
• MyVariant Identifiers: chr6:g.36922695C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36954919C>T , CM000668.2:g.36954919C>T	GRCh38
NC_000006.11:g.36922695C>T , CM000668.1:g.36922695C>T	GRCh37
NC_000006.10:g.37030673C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373674.4:c.159C>T MANE Select	ENSP00000362778.3:p.Asp53=
ENST00000647861.1:c.159C>T	ENSP00000497550.1:p.Asp53=
ENST00000373674.3:c.159C>T	ENSP00000362778.3:p.Asp53=
ENST00000611814.4:c.159C>T	ENSP00000478888.1:p.Asp53=
NM_001199159.1:c.159C>T	NP_001186088.1:p.Asp53=
NM_153370.2:c.159C>T	NP_699201.2:p.Asp53=
XM_005248917.1:c.159C>T	XP_005248974.1:p.Asp53=
XM_011514375.1:c.159C>T	XP_011512677.1:p.Asp53=
XM_005248917.3:c.159C>T	XP_005248974.1:p.Asp53=
XM_011514375.3:c.159C>T	XP_011512677.1:p.Asp53=
XM_017010430.2:c.159C>T	XP_016865919.1:p.Asp53=
NM_153370.3:c.159C>T MANE Select	NP_699201.2:p.Asp53=
NM_001199159.2:c.159C>T	NP_001186088.1:p.Asp53=