Canonical Allele Identifier: CA2692135194

Gene: HMCN2

Linked Data

• gnomAD v4: 9-130433162-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130433162T>G , CM000671.2:g.130433162T>G	GRCh38
NC_000009.11:g.133308549T>G , CM000671.1:g.133308549T>G	GRCh37
NC_000009.10:g.132298370T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624552.4:c.14838-186T>G	ENSP00000485357.2:n.14838-186T>G
ENST00000683500.2:c.14895-186T>G MANE Select	ENSP00000508292.2:n.14895-186T>G
ENST00000623487.1:n.3055T>G
ENST00000624552.3:c.14835-186T>G	ENSP00000485357.1:n.14835-186T>G
NM_001291815.1:c.14895-186T>G	NP_001278744.1:n.14895-186T>G
XM_011518465.1:c.14772-186T>G	XP_011516767.1:n.14772-186T>G
XM_011518466.1:c.14763-186T>G	XP_011516768.1:n.14763-186T>G
XM_011518467.1:c.14718-186T>G	XP_011516769.1:n.14718-186T>G
NM_001291815.2:c.14895-186T>G MANE Select	NP_001278744.1:n.14895-186T>G
XM_011518465.2:c.14772-186T>G	XP_011516767.1:n.14772-186T>G
XM_011518466.2:c.14763-186T>G	XP_011516768.1:n.14763-186T>G
XM_011518467.2:c.14718-186T>G	XP_011516769.1:n.14718-186T>G
XM_017014585.1:c.11676-186T>G	XP_016870074.1:n.11676-186T>G
XM_017014586.1:c.7473-186T>G	XP_016870075.1:n.7473-186T>G
XR_001746957.1:n.92+459A>C
XR_001746958.1:n.92+459A>C