Canonical Allele Identifier: CA728673314
Gene: HMCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1244091163

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185994771A>G , CM000663.2:g.185994771A>G GRCh38
NC_000001.10:g.185963903A>G , CM000663.1:g.185963903A>G GRCh37
NC_000001.9:g.184230526A>G NCBI36
NG_011841.1:g.265221A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.3506-44A>G MANE Select ENSP00000271588.4:n.3506-44A>G
ENST00000271588.8:c.3506-44A>G ENSP00000271588.4:n.3506-44A>G
NM_031935.2:c.3506-44A>G NP_114141.2:n.3506-44A>G
XM_011510037.1:c.3506-44A>G XP_011508339.1:n.3506-44A>G
XM_011510038.1:c.3506-44A>G XP_011508340.1:n.3506-44A>G
XM_011510039.1:c.3506-44A>G XP_011508341.1:n.3506-44A>G
XM_011510040.1:c.3506-44A>G XP_011508342.1:n.3506-44A>G
XM_011510041.1:c.3506-44A>G XP_011508343.1:n.3506-44A>G
XM_011510038.3:c.3506-44A>G XP_011508340.1:n.3506-44A>G
XM_011510041.3:c.3506-44A>G XP_011508343.1:n.3506-44A>G
XM_017002437.1:c.1529-44A>G XP_016857926.1:n.1529-44A>G
XM_024450118.1:c.3506-44A>G XP_024305886.1:n.3506-44A>G
NM_031935.3:c.3506-44A>G MANE Select NP_114141.2:n.3506-44A>G