Canonical Allele Identifier: CA375219475

Gene: HMCN2

Linked Data

• dbSNP Id: rs1734269679
• MyVariant Identifiers: chr9:g.133308821T>G (hg19) ; chr9:g.130433434T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433434T>G , CM000671.2:g.130433434T>G	GRCh38
NC_000009.11:g.133308821T>G , CM000671.1:g.133308821T>G	GRCh37
NC_000009.10:g.132298642T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14924T>G	ENSP00000485357.2:p.Val4975Gly
ENST00000683500.2:c.14981T>G MANE Select	ENSP00000508292.2:p.Val4994Gly
ENST00000623487.1:n.3327T>G
ENST00000624552.3:c.14921T>G	ENSP00000485357.1:p.Val4974Gly
NM_001291815.1:c.14981T>G	NP_001278744.1:p.Val4994Gly
XM_011518465.1:c.14858T>G	XP_011516767.1:p.Val4953Gly
XM_011518466.1:c.14849T>G	XP_011516768.1:p.Val4950Gly
XM_011518467.1:c.14804T>G	XP_011516769.1:p.Val4935Gly
NM_001291815.2:c.14981T>G MANE Select	NP_001278744.1:p.Val4994Gly
XM_011518465.2:c.14858T>G	XP_011516767.1:p.Val4953Gly
XM_011518466.2:c.14849T>G	XP_011516768.1:p.Val4950Gly
XM_011518467.2:c.14804T>G	XP_011516769.1:p.Val4935Gly
XM_017014585.1:c.11762T>G	XP_016870074.1:p.Val3921Gly
XM_017014586.1:c.7559T>G	XP_016870075.1:p.Val2520Gly
XR_001746957.1:n.92+187A>C
XR_001746958.1:n.92+187A>C