Canonical Allele Identifier: CA640857329
Gene: ANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1227380110
gnomAD v2: X-8700118-G-A
gnomAD v3: X-8732077-G-A
gnomAD v4: X-8732077-G-A
MyVariant Identifiers: chrX:g.8700118G>A (hg19) chrX:g.8732077G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732077G>A , CM000685.2:g.8732077G>A GRCh38
NC_000023.10:g.8700118G>A , CM000685.1:g.8700118G>A GRCh37
NC_000023.9:g.8660118G>A NCBI36
NG_007088.1:g.5110C>T
NG_007088.2:g.5110C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.-41C>T MANE Select ENSP00000262648.3:n.-41C>T
ENST00000262648.7:c.-41C>T ENSP00000262648.3:n.-41C>T
ENST00000619786.1:c.-41C>T ENSP00000478734.1:n.-41C>T
NM_000216.2:c.-41C>T NP_000207.2:n.-41C>T
XM_005274501.3:c.-41C>T XP_005274558.1:n.-41C>T
NM_000216.3:c.-41C>T NP_000207.2:n.-41C>T
XM_005274501.4:c.-41C>T XP_005274558.1:n.-41C>T
NM_000216.4:c.-41C>T MANE Select NP_000207.2:n.-41C>T
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