Canonical Allele Identifier: CA449982076

Gene: PI16

Linked Data

• gnomAD v4: 6-36954817-G-A
• MyVariant Identifiers: chr6:g.36922593G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36954817G>A , CM000668.2:g.36954817G>A	GRCh38
NC_000006.11:g.36922593G>A , CM000668.1:g.36922593G>A	GRCh37
NC_000006.10:g.37030571G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373674.4:c.57G>A MANE Select	ENSP00000362778.3:p.Val19=
ENST00000647861.1:c.57G>A	ENSP00000497550.1:p.Val19=
ENST00000373674.3:c.57G>A	ENSP00000362778.3:p.Val19=
ENST00000611814.4:c.57G>A	ENSP00000478888.1:p.Val19=
NM_001199159.1:c.57G>A	NP_001186088.1:p.Val19=
NM_153370.2:c.57G>A	NP_699201.2:p.Val19=
XM_005248917.1:c.57G>A	XP_005248974.1:p.Val19=
XM_011514375.1:c.57G>A	XP_011512677.1:p.Val19=
XM_005248917.3:c.57G>A	XP_005248974.1:p.Val19=
XM_011514375.3:c.57G>A	XP_011512677.1:p.Val19=
XM_017010430.2:c.57G>A	XP_016865919.1:p.Val19=
NM_153370.3:c.57G>A MANE Select	NP_699201.2:p.Val19=
NM_001199159.2:c.57G>A	NP_001186088.1:p.Val19=