Canonical Allele Identifier: CA2838344633
Gene: INTS4P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.65220674A>T , CM000669.2:g.65220674A>T GRCh38
NC_000007.13:g.64681052A>T , CM000669.1:g.64681052A>T GRCh37
NC_000007.12:g.64318487A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000587624.6:n.1437+10861A>T
ENST00000641008.1:n.2024+7880A>T
ENST00000587624.5:n.1437+10861A>T
XR_928285.1:n.1919+7880A>T
NR_146905.1:n.1632+10861A>T
NR_146906.1:n.2146+7880A>T