Canonical Allele Identifier: CA2614617876
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483008T>C , CM000673.2:g.67483008T>C GRCh38
NC_000011.9:g.67250479T>C , CM000673.1:g.67250479T>C GRCh37
NC_000011.8:g.67007055T>C NCBI36
NG_008969.1:g.4975T>C , LRG_460:g.4975T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-151T>C ENSP00000507935.1:n.-151T>C
XM_024448761.1:c.-151T>C XP_024304529.1:n.-151T>C