Canonical Allele Identifier: CA129882505
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs879569069
gnomAD v2: 5-150480346-T-C
gnomAD v3: 5-151100785-T-C
gnomAD v4: 5-151100785-T-C
MyVariant Identifiers: chr5:g.150480346T>C (hg19) chr5:g.151100785T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100785T>C , CM000667.2:g.151100785T>C GRCh38
NC_000005.9:g.150480346T>C , CM000667.1:g.150480346T>C GRCh37
NC_000005.8:g.150460539T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*663A>G MANE Select ENSP00000346550.5:n.*663A>G
ENST00000522664.5:c.378A>G
NM_001155.4:c.*663A>G NP_001146.2:n.*663A>G
NM_001193544.1:c.*663A>G NP_001180473.1:n.*663A>G
NM_001363114.1:c.*663A>G NP_001350043.1:n.*663A>G
NM_001155.5:c.*663A>G MANE Select NP_001146.2:n.*663A>G
NM_001193544.2:c.*663A>G NP_001180473.1:n.*663A>G
NM_001363114.2:c.*663A>G NP_001350043.1:n.*663A>G
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