Canonical Allele Identifier: CA467387264

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308846C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433459C>G , CM000671.2:g.130433459C>G	GRCh38
NC_000009.11:g.133308846C>G , CM000671.1:g.133308846C>G	GRCh37
NC_000009.10:g.132298667C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14949C>G	ENSP00000485357.2:p.Arg4983=
ENST00000683500.2:c.15006C>G MANE Select	ENSP00000508292.2:p.Arg5002=
ENST00000623487.1:n.3352C>G
ENST00000624552.3:c.14946C>G	ENSP00000485357.1:p.Arg4982=
NM_001291815.1:c.15006C>G	NP_001278744.1:p.Arg5002=
XM_011518465.1:c.14883C>G	XP_011516767.1:p.Arg4961=
XM_011518466.1:c.14874C>G	XP_011516768.1:p.Arg4958=
XM_011518467.1:c.14829C>G	XP_011516769.1:p.Arg4943=
NM_001291815.2:c.15006C>G MANE Select	NP_001278744.1:p.Arg5002=
XM_011518465.2:c.14883C>G	XP_011516767.1:p.Arg4961=
XM_011518466.2:c.14874C>G	XP_011516768.1:p.Arg4958=
XM_011518467.2:c.14829C>G	XP_011516769.1:p.Arg4943=
XM_017014585.1:c.11787C>G	XP_016870074.1:p.Arg3929=
XM_017014586.1:c.7584C>G	XP_016870075.1:p.Arg2528=
XR_001746957.1:n.92+162G>C
XR_001746958.1:n.92+162G>C