Canonical Allele Identifier: CA432619157
Gene: COL6A4P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.15216609C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15175102C>G , CM000665.2:g.15175102C>G GRCh38
NC_000003.11:g.15216609C>G , CM000665.1:g.15216609C>G GRCh37
NC_000003.10:g.15191613C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000446690.2:n.1102G>C
ENST00000487147.5:n.926G>C
ENST00000491915.1:n.2G>C
NR_027927.1:n.1102G>C
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