Canonical Allele Identifier: CA805671562
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1323337107

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100911T>A , CM000667.2:g.151100911T>A GRCh38
NC_000005.9:g.150480472T>A , CM000667.1:g.150480472T>A GRCh37
NC_000005.8:g.150460665T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*537A>T MANE Select ENSP00000346550.5:n.*537A>T
ENST00000522664.5:c.252A>T
NM_001155.4:c.*537A>T NP_001146.2:n.*537A>T
NM_001193544.1:c.*537A>T NP_001180473.1:n.*537A>T
NM_001363114.1:c.*537A>T NP_001350043.1:n.*537A>T
NM_001155.5:c.*537A>T MANE Select NP_001146.2:n.*537A>T
NM_001193544.2:c.*537A>T NP_001180473.1:n.*537A>T
NM_001363114.2:c.*537A>T NP_001350043.1:n.*537A>T