Canonical Allele Identifier: CA33457635
Gene: HMCN1 HGNC NCBI

Linked Data

dbSNP Id: rs536361302

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186122845G>T , CM000663.2:g.186122845G>T GRCh38
NC_000001.10:g.186091977G>T , CM000663.1:g.186091977G>T GRCh37
NC_000001.9:g.184358600G>T NCBI36
NG_011841.1:g.393295G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271588.9:c.12230-106G>T MANE Select ENSP00000271588.4:n.12230-106G>T
ENST00000271588.8:c.12230-106G>T ENSP00000271588.4:n.12230-106G>T
NM_031935.2:c.12230-106G>T NP_114141.2:n.12230-106G>T
XM_011510037.1:c.11945-106G>T XP_011508339.1:n.11945-106G>T
XM_011510038.1:c.12230-106G>T XP_011508340.1:n.12230-106G>T
XM_011510039.1:c.12230-106G>T XP_011508341.1:n.12230-106G>T
XM_011510038.3:c.12230-106G>T XP_011508340.1:n.12230-106G>T
XM_017002437.1:c.10253-106G>T XP_016857926.1:n.10253-106G>T
NM_031935.3:c.12230-106G>T MANE Select NP_114141.2:n.12230-106G>T