Canonical Allele Identifier: CA432619105
Gene: COL6A4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.15216604T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175097T>C , CM000665.2:g.15175097T>C GRCh38
NC_000003.11:g.15216604T>C , CM000665.1:g.15216604T>C GRCh37
NC_000003.10:g.15191608T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000446690.2:n.1107A>G
ENST00000487147.5:n.931A>G
ENST00000491915.1:n.7A>G
NR_027927.1:n.1107A>G