Canonical Allele Identifier: CA375219419

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433421-C-G
• MyVariant Identifiers: chr9:g.133308808C>G (hg19) ; chr9:g.130433421C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433421C>G , CM000671.2:g.130433421C>G	GRCh38
NC_000009.11:g.133308808C>G , CM000671.1:g.133308808C>G	GRCh37
NC_000009.10:g.132298629C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14911C>G	ENSP00000485357.2:p.Leu4971Val
ENST00000683500.2:c.14968C>G MANE Select	ENSP00000508292.2:p.Leu4990Val
ENST00000623487.1:n.3314C>G
ENST00000624552.3:c.14908C>G	ENSP00000485357.1:p.Leu4970Val
NM_001291815.1:c.14968C>G	NP_001278744.1:p.Leu4990Val
XM_011518465.1:c.14845C>G	XP_011516767.1:p.Leu4949Val
XM_011518466.1:c.14836C>G	XP_011516768.1:p.Leu4946Val
XM_011518467.1:c.14791C>G	XP_011516769.1:p.Leu4931Val
NM_001291815.2:c.14968C>G MANE Select	NP_001278744.1:p.Leu4990Val
XM_011518465.2:c.14845C>G	XP_011516767.1:p.Leu4949Val
XM_011518466.2:c.14836C>G	XP_011516768.1:p.Leu4946Val
XM_011518467.2:c.14791C>G	XP_011516769.1:p.Leu4931Val
XM_017014585.1:c.11749C>G	XP_016870074.1:p.Leu3917Val
XM_017014586.1:c.7546C>G	XP_016870075.1:p.Leu2516Val
XR_001746957.1:n.92+200G>C
XR_001746958.1:n.92+200G>C