Canonical Allele Identifier: CA432619129
Gene: COL6A4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.15216606C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175099C>G , CM000665.2:g.15175099C>G GRCh38
NC_000003.11:g.15216606C>G , CM000665.1:g.15216606C>G GRCh37
NC_000003.10:g.15191610C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000446690.2:n.1105G>C
ENST00000487147.5:n.929G>C
ENST00000491915.1:n.5G>C
NR_027927.1:n.1105G>C