Canonical Allele Identifier: CA467387269

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308852C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433465C>G , CM000671.2:g.130433465C>G	GRCh38
NC_000009.11:g.133308852C>G , CM000671.1:g.133308852C>G	GRCh37
NC_000009.10:g.132298673C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14955C>G	ENSP00000485357.2:p.Thr4985=
ENST00000683500.2:c.15012C>G MANE Select	ENSP00000508292.2:p.Thr5004=
ENST00000623487.1:n.3358C>G
ENST00000624552.3:c.14952C>G	ENSP00000485357.1:p.Thr4984=
NM_001291815.1:c.15012C>G	NP_001278744.1:p.Thr5004=
XM_011518465.1:c.14889C>G	XP_011516767.1:p.Thr4963=
XM_011518466.1:c.14880C>G	XP_011516768.1:p.Thr4960=
XM_011518467.1:c.14835C>G	XP_011516769.1:p.Thr4945=
NM_001291815.2:c.15012C>G MANE Select	NP_001278744.1:p.Thr5004=
XM_011518465.2:c.14889C>G	XP_011516767.1:p.Thr4963=
XM_011518466.2:c.14880C>G	XP_011516768.1:p.Thr4960=
XM_011518467.2:c.14835C>G	XP_011516769.1:p.Thr4945=
XM_017014585.1:c.11793C>G	XP_016870074.1:p.Thr3931=
XM_017014586.1:c.7590C>G	XP_016870075.1:p.Thr2530=
XR_001746957.1:n.92+156G>C
XR_001746958.1:n.92+156G>C