Canonical Allele Identifier: CA2118892872
Gene: COL4A2 HGNC NCBI

Linked Data

dbSNP Id: rs1594106406
gnomAD v4: 13-110492019-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110492019A>G , CM000675.2:g.110492019A>G GRCh38
NC_000013.10:g.111144366A>G , CM000675.1:g.111144366A>G GRCh37
NC_000013.9:g.109942367A>G NCBI36
NG_032137.1:g.189736A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360467.7:c.3455-51A>G MANE Select ENSP00000353654.5:n.3455-51A>G
ENST00000650225.1:n.1110-51A>G
ENST00000360467.5:c.3455-51A>G ENSP00000353654.5:n.3455-51A>G
NM_001846.2:c.3455-51A>G NP_001837.2:n.3455-51A>G
NM_001846.3:c.3455-51A>G NP_001837.2:n.3455-51A>G
NM_001846.4:c.3455-51A>G MANE Select NP_001837.2:n.3455-51A>G
Search 100 bp 5'
Search 100 bp 3'