Canonical Allele Identifier: CA563603950
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1390829980
gnomAD v2: 5-150480602-C-T
gnomAD v3: 5-151101041-C-T
gnomAD v4: 5-151101041-C-T
MyVariant Identifiers: chr5:g.150480602C>T (hg19) chr5:g.151101041C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101041C>T , CM000667.2:g.151101041C>T GRCh38
NC_000005.9:g.150480602C>T , CM000667.1:g.150480602C>T GRCh37
NC_000005.8:g.150460795C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*407G>A MANE Select ENSP00000346550.5:n.*407G>A
ENST00000522664.5:c.201-79G>A
NM_001155.4:c.*407G>A NP_001146.2:n.*407G>A
NM_001193544.1:c.*407G>A NP_001180473.1:n.*407G>A
NM_001363114.1:c.*407G>A NP_001350043.1:n.*407G>A
NM_001155.5:c.*407G>A MANE Select NP_001146.2:n.*407G>A
NM_001193544.2:c.*407G>A NP_001180473.1:n.*407G>A
NM_001363114.2:c.*407G>A NP_001350043.1:n.*407G>A
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