Canonical Allele Identifier: CA432619137
Gene: COL6A4P1 HGNC NCBI

Linked Data

dbSNP Id: rs2125215786
MyVariant Identifiers: chr3:g.15216607C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175100C>A , CM000665.2:g.15175100C>A GRCh38
NC_000003.11:g.15216607C>A , CM000665.1:g.15216607C>A GRCh37
NC_000003.10:g.15191611C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000446690.2:n.1104G>T
ENST00000487147.5:n.928G>T
ENST00000491915.1:n.4G>T
NR_027927.1:n.1104G>T
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