Canonical Allele Identifier: CA375219517

Gene: HMCN2

Linked Data

• MyVariant Identifiers: chr9:g.133308832C>G (hg19) ; chr9:g.130433445C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433445C>G , CM000671.2:g.130433445C>G	GRCh38
NC_000009.11:g.133308832C>G , CM000671.1:g.133308832C>G	GRCh37
NC_000009.10:g.132298653C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14935C>G	ENSP00000485357.2:p.His4979Asp
ENST00000683500.2:c.14992C>G MANE Select	ENSP00000508292.2:p.His4998Asp
ENST00000623487.1:n.3338C>G
ENST00000624552.3:c.14932C>G	ENSP00000485357.1:p.His4978Asp
NM_001291815.1:c.14992C>G	NP_001278744.1:p.His4998Asp
XM_011518465.1:c.14869C>G	XP_011516767.1:p.His4957Asp
XM_011518466.1:c.14860C>G	XP_011516768.1:p.His4954Asp
XM_011518467.1:c.14815C>G	XP_011516769.1:p.His4939Asp
NM_001291815.2:c.14992C>G MANE Select	NP_001278744.1:p.His4998Asp
XM_011518465.2:c.14869C>G	XP_011516767.1:p.His4957Asp
XM_011518466.2:c.14860C>G	XP_011516768.1:p.His4954Asp
XM_011518467.2:c.14815C>G	XP_011516769.1:p.His4939Asp
XM_017014585.1:c.11773C>G	XP_016870074.1:p.His3925Asp
XM_017014586.1:c.7570C>G	XP_016870075.1:p.His2524Asp
XR_001746957.1:n.92+176G>C
XR_001746958.1:n.92+176G>C