Canonical Allele Identifier: CA33440079
Gene: HMCN1 HGNC NCBI

Linked Data

dbSNP Id: rs779530809

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.185994770G>T , CM000663.2:g.185994770G>T GRCh38
NC_000001.10:g.185963902G>T , CM000663.1:g.185963902G>T GRCh37
NC_000001.9:g.184230525G>T NCBI36
NG_011841.1:g.265220G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.3506-45G>T MANE Select ENSP00000271588.4:n.3506-45G>T
ENST00000271588.8:c.3506-45G>T ENSP00000271588.4:n.3506-45G>T
NM_031935.2:c.3506-45G>T NP_114141.2:n.3506-45G>T
XM_011510037.1:c.3506-45G>T XP_011508339.1:n.3506-45G>T
XM_011510038.1:c.3506-45G>T XP_011508340.1:n.3506-45G>T
XM_011510039.1:c.3506-45G>T XP_011508341.1:n.3506-45G>T
XM_011510040.1:c.3506-45G>T XP_011508342.1:n.3506-45G>T
XM_011510041.1:c.3506-45G>T XP_011508343.1:n.3506-45G>T
XM_011510038.3:c.3506-45G>T XP_011508340.1:n.3506-45G>T
XM_011510041.3:c.3506-45G>T XP_011508343.1:n.3506-45G>T
XM_017002437.1:c.1529-45G>T XP_016857926.1:n.1529-45G>T
XM_024450118.1:c.3506-45G>T XP_024305886.1:n.3506-45G>T
NM_031935.3:c.3506-45G>T MANE Select NP_114141.2:n.3506-45G>T