Canonical Allele Identifier: CA375219329
Gene: HMCN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433398C>G , CM000671.2:g.130433398C>G GRCh38
NC_000009.11:g.133308785C>G , CM000671.1:g.133308785C>G GRCh37
NC_000009.10:g.132298606C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14888C>G ENSP00000485357.2:p.Thr4963Arg
ENST00000683500.2:c.14945C>G MANE Select ENSP00000508292.2:p.Thr4982Arg
ENST00000623487.1:n.3291C>G
ENST00000624552.3:c.14885C>G ENSP00000485357.1:p.Thr4962Arg
NM_001291815.1:c.14945C>G NP_001278744.1:p.Thr4982Arg
XM_011518465.1:c.14822C>G XP_011516767.1:p.Thr4941Arg
XM_011518466.1:c.14813C>G XP_011516768.1:p.Thr4938Arg
XM_011518467.1:c.14768C>G XP_011516769.1:p.Thr4923Arg
NM_001291815.2:c.14945C>G MANE Select NP_001278744.1:p.Thr4982Arg
XM_011518465.2:c.14822C>G XP_011516767.1:p.Thr4941Arg
XM_011518466.2:c.14813C>G XP_011516768.1:p.Thr4938Arg
XM_011518467.2:c.14768C>G XP_011516769.1:p.Thr4923Arg
XM_017014585.1:c.11726C>G XP_016870074.1:p.Thr3909Arg
XM_017014586.1:c.7523C>G XP_016870075.1:p.Thr2508Arg
XR_001746957.1:n.92+223G>C
XR_001746958.1:n.92+223G>C