Canonical Allele Identifier: CA449982149

Gene: PI16

Linked Data

• MyVariant Identifiers: chr6:g.36922692A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36954916A>C , CM000668.2:g.36954916A>C	GRCh38
NC_000006.11:g.36922692A>C , CM000668.1:g.36922692A>C	GRCh37
NC_000006.10:g.37030670A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373674.4:c.156A>C MANE Select	ENSP00000362778.3:p.Ser52=
ENST00000647861.1:c.156A>C	ENSP00000497550.1:p.Ser52=
ENST00000373674.3:c.156A>C	ENSP00000362778.3:p.Ser52=
ENST00000611814.4:c.156A>C	ENSP00000478888.1:p.Ser52=
NM_001199159.1:c.156A>C	NP_001186088.1:p.Ser52=
NM_153370.2:c.156A>C	NP_699201.2:p.Ser52=
XM_005248917.1:c.156A>C	XP_005248974.1:p.Ser52=
XM_011514375.1:c.156A>C	XP_011512677.1:p.Ser52=
XM_005248917.3:c.156A>C	XP_005248974.1:p.Ser52=
XM_011514375.3:c.156A>C	XP_011512677.1:p.Ser52=
XM_017010430.2:c.156A>C	XP_016865919.1:p.Ser52=
NM_153370.3:c.156A>C MANE Select	NP_699201.2:p.Ser52=
NM_001199159.2:c.156A>C	NP_001186088.1:p.Ser52=