Canonical Allele Identifier: CA1881265729
Gene: HMCN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130432953T= , CM000671.2:g.130432953T= GRCh38
NC_000009.11:g.133308340T= , CM000671.1:g.133308340T= GRCh37
NC_000009.10:g.132298161T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624552.4:c.14838-395T= ENSP00000485357.2:n.14838-395T=
ENST00000683500.2:c.14895-395T= MANE Select ENSP00000508292.2:n.14895-395T=
ENST00000623487.1:n.2846T=
ENST00000624552.3:c.14835-395T= ENSP00000485357.1:n.14835-395T=
NM_001291815.1:c.14895-395T= NP_001278744.1:n.14895-395T=
XM_011518465.1:c.14772-395T= XP_011516767.1:n.14772-395T=
XM_011518466.1:c.14763-395T= XP_011516768.1:n.14763-395T=
XM_011518467.1:c.14718-395T= XP_011516769.1:n.14718-395T=
NM_001291815.2:c.14895-395T= MANE Select NP_001278744.1:n.14895-395T=
XM_011518465.2:c.14772-395T= XP_011516767.1:n.14772-395T=
XM_011518466.2:c.14763-395T= XP_011516768.1:n.14763-395T=
XM_011518467.2:c.14718-395T= XP_011516769.1:n.14718-395T=
XM_017014585.1:c.11676-395T= XP_016870074.1:n.11676-395T=
XM_017014586.1:c.7473-395T= XP_016870075.1:n.7473-395T=
XR_001746957.1:n.92+668A=
XR_001746958.1:n.92+668A=