Canonical Allele Identifier: CA467387254

Gene: HMCN2

Linked Data

• dbSNP Id: rs1356704438
• gnomAD v2: 9-133308831-C-T
• gnomAD v3: 9-130433444-C-T
• gnomAD v4: 9-130433444-C-T
• MyVariant Identifiers: chr9:g.133308831C>T (hg19) ; chr9:g.130433444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433444C>T , CM000671.2:g.130433444C>T	GRCh38
NC_000009.11:g.133308831C>T , CM000671.1:g.133308831C>T	GRCh37
NC_000009.10:g.132298652C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14934C>T	ENSP00000485357.2:p.His4978=
ENST00000683500.2:c.14991C>T MANE Select	ENSP00000508292.2:p.His4997=
ENST00000623487.1:n.3337C>T
ENST00000624552.3:c.14931C>T	ENSP00000485357.1:p.His4977=
NM_001291815.1:c.14991C>T	NP_001278744.1:p.His4997=
XM_011518465.1:c.14868C>T	XP_011516767.1:p.His4956=
XM_011518466.1:c.14859C>T	XP_011516768.1:p.His4953=
XM_011518467.1:c.14814C>T	XP_011516769.1:p.His4938=
NM_001291815.2:c.14991C>T MANE Select	NP_001278744.1:p.His4997=
XM_011518465.2:c.14868C>T	XP_011516767.1:p.His4956=
XM_011518466.2:c.14859C>T	XP_011516768.1:p.His4953=
XM_011518467.2:c.14814C>T	XP_011516769.1:p.His4938=
XM_017014585.1:c.11772C>T	XP_016870074.1:p.His3924=
XM_017014586.1:c.7569C>T	XP_016870075.1:p.His2523=
XR_001746957.1:n.92+177G>A
XR_001746958.1:n.92+177G>A