Canonical Allele Identifier: CA375219306

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308781T>G (hg19) ; chr9:g.130433394T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433394T>G , CM000671.2:g.130433394T>G	GRCh38
NC_000009.11:g.133308781T>G , CM000671.1:g.133308781T>G	GRCh37
NC_000009.10:g.132298602T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14884T>G	ENSP00000485357.2:p.Ser4962Ala
ENST00000683500.2:c.14941T>G MANE Select	ENSP00000508292.2:p.Ser4981Ala
ENST00000623487.1:n.3287T>G
ENST00000624552.3:c.14881T>G	ENSP00000485357.1:p.Ser4961Ala
NM_001291815.1:c.14941T>G	NP_001278744.1:p.Ser4981Ala
XM_011518465.1:c.14818T>G	XP_011516767.1:p.Ser4940Ala
XM_011518466.1:c.14809T>G	XP_011516768.1:p.Ser4937Ala
XM_011518467.1:c.14764T>G	XP_011516769.1:p.Ser4922Ala
NM_001291815.2:c.14941T>G MANE Select	NP_001278744.1:p.Ser4981Ala
XM_011518465.2:c.14818T>G	XP_011516767.1:p.Ser4940Ala
XM_011518466.2:c.14809T>G	XP_011516768.1:p.Ser4937Ala
XM_011518467.2:c.14764T>G	XP_011516769.1:p.Ser4922Ala
XM_017014585.1:c.11722T>G	XP_016870074.1:p.Ser3908Ala
XM_017014586.1:c.7519T>G	XP_016870075.1:p.Ser2507Ala
XR_001746957.1:n.92+227A>C
XR_001746958.1:n.92+227A>C