Canonical Allele Identifier: CA1881266237
Gene: HMCN2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14884T= ENSP00000485357.2:p.Ser4962=
ENST00000683500.2:c.14941T= MANE Select ENSP00000508292.2:p.Ser4981=
ENST00000623487.1:n.3287T=
ENST00000624552.3:c.14881T= ENSP00000485357.1:p.Ser4961=
NM_001291815.1:c.14941T= NP_001278744.1:p.Ser4981=
XM_011518465.1:c.14818T= XP_011516767.1:p.Ser4940=
XM_011518466.1:c.14809T= XP_011516768.1:p.Ser4937=
XM_011518467.1:c.14764T= XP_011516769.1:p.Ser4922=
NM_001291815.2:c.14941T= MANE Select NP_001278744.1:p.Ser4981=
XM_011518465.2:c.14818T= XP_011516767.1:p.Ser4940=
XM_011518466.2:c.14809T= XP_011516768.1:p.Ser4937=
XM_011518467.2:c.14764T= XP_011516769.1:p.Ser4922=
XM_017014585.1:c.11722T= XP_016870074.1:p.Ser3908=
XM_017014586.1:c.7519T= XP_016870075.1:p.Ser2507=
XR_001746957.1:n.92+227A=
XR_001746958.1:n.92+227A=