Canonical Allele Identifier: CA805671690
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1294513453
gnomAD v4: 5-151101066-T-G
MyVariant Identifiers: chr5:g.150480627T>G (hg19) chr5:g.151101066T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101066T>G , CM000667.2:g.151101066T>G GRCh38
NC_000005.9:g.150480627T>G , CM000667.1:g.150480627T>G GRCh37
NC_000005.8:g.150460820T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*382A>C MANE Select ENSP00000346550.5:n.*382A>C
ENST00000522664.5:c.201-104A>C
NM_001155.4:c.*382A>C NP_001146.2:n.*382A>C
NM_001193544.1:c.*382A>C NP_001180473.1:n.*382A>C
NM_001363114.1:c.*382A>C NP_001350043.1:n.*382A>C
NM_001155.5:c.*382A>C MANE Select NP_001146.2:n.*382A>C
NM_001193544.2:c.*382A>C NP_001180473.1:n.*382A>C
NM_001363114.2:c.*382A>C NP_001350043.1:n.*382A>C
Search 100 bp 5'
Search 100 bp 3'