Canonical Allele Identifier: CA432619162
Gene: COL6A4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.15216610C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175103C>T , CM000665.2:g.15175103C>T GRCh38
NC_000003.11:g.15216610C>T , CM000665.1:g.15216610C>T GRCh37
NC_000003.10:g.15191614C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000446690.2:n.1101G>A
ENST00000487147.5:n.925G>A
ENST00000491915.1:n.1G>A
NR_027927.1:n.1101G>A
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