Canonical Allele Identifier: CA467387252

Gene: HMCN2

Linked Data

• dbSNP Id: rs1844888193
• MyVariant Identifiers: chr9:g.133308828C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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