Canonical Allele Identifier: CA375219628

Gene: HMCN2

Linked Data

• dbSNP Id: rs1164448811
• gnomAD v2: 9-133308860-C-G
• gnomAD v4: 9-130433473-C-G
• MyVariant Identifiers: chr9:g.133308860C>G (hg19) ; chr9:g.130433473C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433473C>G , CM000671.2:g.130433473C>G	GRCh38
NC_000009.11:g.133308860C>G , CM000671.1:g.133308860C>G	GRCh37
NC_000009.10:g.132298681C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14963C>G	ENSP00000485357.2:p.Ser4988Cys
ENST00000683500.2:c.15020C>G MANE Select	ENSP00000508292.2:p.Ser5007Cys
ENST00000623487.1:n.3366C>G
ENST00000624552.3:c.14960C>G	ENSP00000485357.1:p.Ser4987Cys
NM_001291815.1:c.15020C>G	NP_001278744.1:p.Ser5007Cys
XM_011518465.1:c.14897C>G	XP_011516767.1:p.Ser4966Cys
XM_011518466.1:c.14888C>G	XP_011516768.1:p.Ser4963Cys
XM_011518467.1:c.14843C>G	XP_011516769.1:p.Ser4948Cys
NM_001291815.2:c.15020C>G MANE Select	NP_001278744.1:p.Ser5007Cys
XM_011518465.2:c.14897C>G	XP_011516767.1:p.Ser4966Cys
XM_011518466.2:c.14888C>G	XP_011516768.1:p.Ser4963Cys
XM_011518467.2:c.14843C>G	XP_011516769.1:p.Ser4948Cys
XM_017014585.1:c.11801C>G	XP_016870074.1:p.Ser3934Cys
XM_017014586.1:c.7598C>G	XP_016870075.1:p.Ser2533Cys
XR_001746957.1:n.92+148G>C
XR_001746958.1:n.92+148G>C