Canonical Allele Identifier: CA960161729
Gene: COL4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1877779898
gnomAD v3: 13-110174377-T-C
gnomAD v4: 13-110174377-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110174377T>C , CM000675.2:g.110174377T>C GRCh38
NC_000013.10:g.110826724T>C , CM000675.1:g.110826724T>C GRCh37
NC_000013.9:g.109624725T>C NCBI36
NG_011544.2:g.137773A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3406+69A>G MANE Select ENSP00000364979.4:n.3406+69A>G
ENST00000375820.8:c.3406+69A>G ENSP00000364979.4:n.3406+69A>G
NM_001845.5:c.3406+69A>G NP_001836.3:n.3406+69A>G
XM_011521048.1:c.3214+69A>G XP_011519350.1:n.3214+69A>G
XM_011521048.2:c.3214+69A>G XP_011519350.1:n.3214+69A>G
NM_001845.6:c.3406+69A>G MANE Select NP_001836.3:n.3406+69A>G
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