Canonical Allele Identifier: CA2692135194
Gene: HMCN2 HGNC NCBI

Linked Data

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