Canonical Allele Identifier: CA2392171519
Gene: COL18A1 HGNC NCBI

Linked Data

dbSNP Id: rs562399558

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45476302C>G , CM000683.2:g.45476302C>G GRCh38
NC_000021.8:g.46896216C>G , CM000683.1:g.46896216C>G GRCh37
NC_000021.7:g.45720644C>G NCBI36
NG_011903.1:g.76120C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355480.10:c.1339-49C>G ENSP00000347665.5:n.1339-49C>G
ENST00000651438.1:c.799-49C>G MANE Select ENSP00000498485.1:n.799-49C>G
ENST00000355480.9:c.1339-49C>G ENSP00000347665.5:n.1339-49C>G
ENST00000359759.8:c.2044-49C>G ENSP00000352798.4:n.2044-49C>G
ENST00000400337.6:c.799-49C>G ENSP00000383191.2:n.799-49C>G
NM_030582.3:c.1339-49C>G NP_085059.2:n.1339-49C>G
NM_130444.2:c.2044-49C>G NP_569711.2:n.2044-49C>G
NM_130445.3:c.799-49C>G NP_569712.2:n.799-49C>G
NM_030582.4:c.1339-49C>G NP_085059.2:n.1339-49C>G
NM_130444.3:c.2044-49C>G NP_569711.2:n.2044-49C>G
NM_130445.4:c.799-49C>G NP_569712.2:n.799-49C>G
NM_001379500.1:c.799-49C>G MANE Select NP_001366429.1:n.799-49C>G