Canonical Allele Identifier: CA432619120
Gene: COL6A4P1 HGNC NCBI

Linked Data

gnomAD v4: 3-15175098-G-T
MyVariant Identifiers: chr3:g.15216605G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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