Canonical Allele Identifier: CA436751420

Gene: MYNN

Linked Data

• MyVariant Identifiers: chr3:g.169502492T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169784704T>C , CM000665.2:g.169784704T>C	GRCh38
NC_000003.11:g.169502492T>C , CM000665.1:g.169502492T>C	GRCh37
NC_000003.10:g.170985186T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349841.10:c.1566T>C MANE Select	ENSP00000326240.4:p.His522=
ENST00000349841.9:c.1566T>C	ENSP00000326240.4:p.His522=
ENST00000356716.8:c.1566T>C	ENSP00000349150.3:p.His522=
ENST00000544106.5:c.1483+1144T>C	ENSP00000440637.1:n.1483+1144T>C
ENST00000602751.5:c.*1174T>C	ENSP00000473654.1:n.*1174T>C
NM_001185118.1:c.1566T>C	NP_001172047.1:p.His522=
NM_001185119.1:c.1483+1144T>C	NP_001172048.1:n.1483+1144T>C
NM_018657.4:c.1566T>C	NP_061127.1:p.His522=
NR_033702.1:n.1865T>C
NR_033703.1:n.1879T>C
XM_005247621.3:c.1482T>C	XP_005247678.1:p.His494=
XM_005247622.3:c.1320T>C	XP_005247679.1:p.His440=
XM_005247624.3:c.1224T>C	XP_005247681.1:p.His408=
XM_011512987.1:c.1566T>C	XP_011511289.1:p.His522=
XM_011512988.1:c.1566T>C	XP_011511290.1:p.His522=
XM_005247621.5:c.1482T>C	XP_005247678.1:p.His494=
XM_005247622.4:c.1320T>C	XP_005247679.1:p.His440=
XM_005247624.4:c.1224T>C	XP_005247681.1:p.His408=
XM_017006864.2:c.1566T>C	XP_016862353.1:p.His522=
XM_017006865.2:c.1140T>C	XP_016862354.1:p.His380=
XM_017006866.2:c.1140T>C	XP_016862355.1:p.His380=
XM_017006867.2:c.747T>C	XP_016862356.1:p.His249=
XM_017006868.2:c.663T>C	XP_016862357.1:p.His221=
XR_002959552.1:n.3398T>C
NM_001185118.2:c.1566T>C	NP_001172047.1:p.His522=
NM_018657.5:c.1566T>C MANE Select	NP_061127.1:p.His522=
NR_033702.2:n.1534T>C
NR_033703.2:n.1548T>C