Canonical Allele Identifier: CA5321362

Gene: FCN2

Linked Data

• dbSNP Id: rs7851696
• ExAC: 9:137779091 G / C
• MyVariant Identifiers: chr9:g.137779091G>C (hg19) ; chr9:g.134887245G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134887245G>C , CM000671.2:g.134887245G>C	GRCh38
NC_000009.11:g.137779091G>C , CM000671.1:g.137779091G>C	GRCh37
NC_000009.10:g.136918912G>C	NCBI36
NG_011649.1:g.11434G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000291744.11:c.772G>C MANE Select	ENSP00000291744.6:p.Ala258Pro
ENST00000291744.10:c.772G>C	ENSP00000291744.6:p.Ala258Pro
ENST00000350339.3:c.658G>C	ENSP00000291741.5:p.Ala220Pro
NM_004108.2:c.772G>C	NP_004099.2:p.Ala258Pro
NM_015837.2:c.658G>C	NP_056652.1:p.Ala220Pro
XM_006717015.2:c.625G>C	XP_006717078.1:p.Ala209Pro
XM_011518392.1:c.739G>C	XP_011516694.1:p.Ala247Pro
XM_006717015.4:c.625G>C	XP_006717078.1:p.Ala209Pro
XM_011518392.3:c.739G>C	XP_011516694.1:p.Ala247Pro
NM_004108.3:c.772G>C MANE Select	NP_004099.2:p.Ala258Pro
NM_015837.3:c.658G>C	NP_056652.1:p.Ala220Pro