Canonical Allele Identifier: CA200583116
Gene: HMCN2 HGNC NCBI

Linked Data

dbSNP Id: rs549817254

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130433399G>C , CM000671.2:g.130433399G>C GRCh38
NC_000009.11:g.133308786G>C , CM000671.1:g.133308786G>C GRCh37
NC_000009.10:g.132298607G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14889G>C ENSP00000485357.2:p.Thr4963=
ENST00000683500.2:c.14946G>C MANE Select ENSP00000508292.2:p.Thr4982=
ENST00000623487.1:n.3292G>C
ENST00000624552.3:c.14886G>C ENSP00000485357.1:p.Thr4962=
NM_001291815.1:c.14946G>C NP_001278744.1:p.Thr4982=
XM_011518465.1:c.14823G>C XP_011516767.1:p.Thr4941=
XM_011518466.1:c.14814G>C XP_011516768.1:p.Thr4938=
XM_011518467.1:c.14769G>C XP_011516769.1:p.Thr4923=
NM_001291815.2:c.14946G>C MANE Select NP_001278744.1:p.Thr4982=
XM_011518465.2:c.14823G>C XP_011516767.1:p.Thr4941=
XM_011518466.2:c.14814G>C XP_011516768.1:p.Thr4938=
XM_011518467.2:c.14769G>C XP_011516769.1:p.Thr4923=
XM_017014585.1:c.11727G>C XP_016870074.1:p.Thr3909=
XM_017014586.1:c.7524G>C XP_016870075.1:p.Thr2508=
XR_001746957.1:n.92+222C>G
XR_001746958.1:n.92+222C>G