Canonical Allele Identifier: CA1118409635
Gene: COLEC10 HGNC NCBI

Linked Data

dbSNP Id: rs1813671669

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119000362A>G , CM000670.2:g.119000362A>G GRCh38
NC_000008.10:g.120012601A>G , CM000670.1:g.120012601A>G GRCh37
NC_000008.9:g.120081782A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521788.1:n.122+4789A>G
XM_005250756.2:c.-60+47984A>G XP_005250813.1:n.-60+47984A>G
NM_001324095.1:c.-323-37074A>G NP_001311024.1:n.-323-37074A>G
XM_005250756.3:c.-60+47984A>G XP_005250813.1:n.-60+47984A>G
NM_001324095.2:c.-323-37074A>G NP_001311024.1:n.-323-37074A>G