Canonical Allele Identifier: CA467387267

Gene: HMCN2

Linked Data

• dbSNP Id: rs1195295717
• gnomAD v2: 9-133308849-C-T
• gnomAD v4: 9-130433462-C-T
• MyVariant Identifiers: chr9:g.133308849C>T (hg19) ; chr9:g.130433462C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433462C>T , CM000671.2:g.130433462C>T	GRCh38
NC_000009.11:g.133308849C>T , CM000671.1:g.133308849C>T	GRCh37
NC_000009.10:g.132298670C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14952C>T	ENSP00000485357.2:p.Leu4984=
ENST00000683500.2:c.15009C>T MANE Select	ENSP00000508292.2:p.Leu5003=
ENST00000623487.1:n.3355C>T
ENST00000624552.3:c.14949C>T	ENSP00000485357.1:p.Leu4983=
NM_001291815.1:c.15009C>T	NP_001278744.1:p.Leu5003=
XM_011518465.1:c.14886C>T	XP_011516767.1:p.Leu4962=
XM_011518466.1:c.14877C>T	XP_011516768.1:p.Leu4959=
XM_011518467.1:c.14832C>T	XP_011516769.1:p.Leu4944=
NM_001291815.2:c.15009C>T MANE Select	NP_001278744.1:p.Leu5003=
XM_011518465.2:c.14886C>T	XP_011516767.1:p.Leu4962=
XM_011518466.2:c.14877C>T	XP_011516768.1:p.Leu4959=
XM_011518467.2:c.14832C>T	XP_011516769.1:p.Leu4944=
XM_017014585.1:c.11790C>T	XP_016870074.1:p.Leu3930=
XM_017014586.1:c.7587C>T	XP_016870075.1:p.Leu2529=
XR_001746957.1:n.92+159G>A
XR_001746958.1:n.92+159G>A