Canonical Allele Identifier: CA1213006421
Gene: HMCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1661460674

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186122875C>A , CM000663.2:g.186122875C>A GRCh38
NC_000001.10:g.186092007C>A , CM000663.1:g.186092007C>A GRCh37
NC_000001.9:g.184358630C>A NCBI36
NG_011841.1:g.393325C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.12230-76C>A MANE Select ENSP00000271588.4:n.12230-76C>A
ENST00000271588.8:c.12230-76C>A ENSP00000271588.4:n.12230-76C>A
NM_031935.2:c.12230-76C>A NP_114141.2:n.12230-76C>A
XM_011510037.1:c.11945-76C>A XP_011508339.1:n.11945-76C>A
XM_011510038.1:c.12230-76C>A XP_011508340.1:n.12230-76C>A
XM_011510039.1:c.12230-76C>A XP_011508341.1:n.12230-76C>A
XM_011510038.3:c.12230-76C>A XP_011508340.1:n.12230-76C>A
XM_017002437.1:c.10253-76C>A XP_016857926.1:n.10253-76C>A
NM_031935.3:c.12230-76C>A MANE Select NP_114141.2:n.12230-76C>A