Canonical Allele Identifier: CA467387244

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308819C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433432C>G , CM000671.2:g.130433432C>G	GRCh38
NC_000009.11:g.133308819C>G , CM000671.1:g.133308819C>G	GRCh37
NC_000009.10:g.132298640C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14922C>G	ENSP00000485357.2:p.Gly4974=
ENST00000683500.2:c.14979C>G MANE Select	ENSP00000508292.2:p.Gly4993=
ENST00000623487.1:n.3325C>G
ENST00000624552.3:c.14919C>G	ENSP00000485357.1:p.Gly4973=
NM_001291815.1:c.14979C>G	NP_001278744.1:p.Gly4993=
XM_011518465.1:c.14856C>G	XP_011516767.1:p.Gly4952=
XM_011518466.1:c.14847C>G	XP_011516768.1:p.Gly4949=
XM_011518467.1:c.14802C>G	XP_011516769.1:p.Gly4934=
NM_001291815.2:c.14979C>G MANE Select	NP_001278744.1:p.Gly4993=
XM_011518465.2:c.14856C>G	XP_011516767.1:p.Gly4952=
XM_011518466.2:c.14847C>G	XP_011516768.1:p.Gly4949=
XM_011518467.2:c.14802C>G	XP_011516769.1:p.Gly4934=
XM_017014585.1:c.11760C>G	XP_016870074.1:p.Gly3920=
XM_017014586.1:c.7557C>G	XP_016870075.1:p.Gly2519=
XR_001746957.1:n.92+189G>C
XR_001746958.1:n.92+189G>C