Canonical Allele Identifier: CA640857326
Gene: ANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1285851331
gnomAD v2: X-8700097-G-C
gnomAD v3: X-8732056-G-C
gnomAD v4: X-8732056-G-C
MyVariant Identifiers: chrX:g.8700097G>C (hg19) chrX:g.8732056G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732056G>C , CM000685.2:g.8732056G>C GRCh38
NC_000023.10:g.8700097G>C , CM000685.1:g.8700097G>C GRCh37
NC_000023.9:g.8660097G>C NCBI36
NG_007088.1:g.5131C>G
NG_007088.2:g.5131C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.-20C>G MANE Select ENSP00000262648.3:n.-20C>G
ENST00000262648.7:c.-20C>G ENSP00000262648.3:n.-20C>G
ENST00000619786.1:c.-20C>G ENSP00000478734.1:n.-20C>G
NM_000216.2:c.-20C>G NP_000207.2:n.-20C>G
XM_005274501.3:c.-20C>G XP_005274558.1:n.-20C>G
NM_000216.3:c.-20C>G NP_000207.2:n.-20C>G
XM_005274501.4:c.-20C>G XP_005274558.1:n.-20C>G
NM_000216.4:c.-20C>G MANE Select NP_000207.2:n.-20C>G
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