Canonical Allele Identifier: CA388661875
Gene: COL4A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736059
ClinVar RCV Id: RCV003557808
MyVariant Identifiers: chr13:g.110822056C>G (hg19) chr13:g.110169709C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110169709C>G , CM000675.2:g.110169709C>G GRCh38
NC_000013.10:g.110822056C>G , CM000675.1:g.110822056C>G GRCh37
NC_000013.9:g.109620057C>G NCBI36
NG_011544.2:g.142441G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3796G>C MANE Select ENSP00000364979.4:p.Gly1266Arg
ENST00000375820.8:c.3796G>C ENSP00000364979.4:p.Gly1266Arg
NM_001845.5:c.3796G>C NP_001836.3:p.Gly1266Arg
XM_011521048.1:c.3604G>C XP_011519350.1:p.Gly1202Arg
XM_011521048.2:c.3604G>C XP_011519350.1:p.Gly1202Arg
NM_001845.6:c.3796G>C MANE Select NP_001836.3:p.Gly1266Arg
Search 100 bp 5'
Search 100 bp 3'