Canonical Allele Identifier: CA432619117
Gene: COL6A4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.15216605G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175098G>C , CM000665.2:g.15175098G>C GRCh38
NC_000003.11:g.15216605G>C , CM000665.1:g.15216605G>C GRCh37
NC_000003.10:g.15191609G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000446690.2:n.1106C>G
ENST00000487147.5:n.930C>G
ENST00000491915.1:n.6C>G
NR_027927.1:n.1106C>G