Canonical Allele Identifier: CA467387253

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308828C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433441C>G , CM000671.2:g.130433441C>G	GRCh38
NC_000009.11:g.133308828C>G , CM000671.1:g.133308828C>G	GRCh37
NC_000009.10:g.132298649C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14931C>G	ENSP00000485357.2:p.Ala4977=
ENST00000683500.2:c.14988C>G MANE Select	ENSP00000508292.2:p.Ala4996=
ENST00000623487.1:n.3334C>G
ENST00000624552.3:c.14928C>G	ENSP00000485357.1:p.Ala4976=
NM_001291815.1:c.14988C>G	NP_001278744.1:p.Ala4996=
XM_011518465.1:c.14865C>G	XP_011516767.1:p.Ala4955=
XM_011518466.1:c.14856C>G	XP_011516768.1:p.Ala4952=
XM_011518467.1:c.14811C>G	XP_011516769.1:p.Ala4937=
NM_001291815.2:c.14988C>G MANE Select	NP_001278744.1:p.Ala4996=
XM_011518465.2:c.14865C>G	XP_011516767.1:p.Ala4955=
XM_011518466.2:c.14856C>G	XP_011516768.1:p.Ala4952=
XM_011518467.2:c.14811C>G	XP_011516769.1:p.Ala4937=
XM_017014585.1:c.11769C>G	XP_016870074.1:p.Ala3923=
XM_017014586.1:c.7566C>G	XP_016870075.1:p.Ala2522=
XR_001746957.1:n.92+180G>C
XR_001746958.1:n.92+180G>C