Canonical Allele Identifier: CA467387239

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433426-C-T
• MyVariant Identifiers: chr9:g.133308813C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433426C>T , CM000671.2:g.130433426C>T	GRCh38
NC_000009.11:g.133308813C>T , CM000671.1:g.133308813C>T	GRCh37
NC_000009.10:g.132298634C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14916C>T	ENSP00000485357.2:p.Pro4972=
ENST00000683500.2:c.14973C>T MANE Select	ENSP00000508292.2:p.Pro4991=
ENST00000623487.1:n.3319C>T
ENST00000624552.3:c.14913C>T	ENSP00000485357.1:p.Pro4971=
NM_001291815.1:c.14973C>T	NP_001278744.1:p.Pro4991=
XM_011518465.1:c.14850C>T	XP_011516767.1:p.Pro4950=
XM_011518466.1:c.14841C>T	XP_011516768.1:p.Pro4947=
XM_011518467.1:c.14796C>T	XP_011516769.1:p.Pro4932=
NM_001291815.2:c.14973C>T MANE Select	NP_001278744.1:p.Pro4991=
XM_011518465.2:c.14850C>T	XP_011516767.1:p.Pro4950=
XM_011518466.2:c.14841C>T	XP_011516768.1:p.Pro4947=
XM_011518467.2:c.14796C>T	XP_011516769.1:p.Pro4932=
XM_017014585.1:c.11754C>T	XP_016870074.1:p.Pro3918=
XM_017014586.1:c.7551C>T	XP_016870075.1:p.Pro2517=
XR_001746957.1:n.92+195G>A
XR_001746958.1:n.92+195G>A