Canonical Allele Identifier: CA2318204682
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs2025057757
gnomAD v4: 19-2251978-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251978C>T , CM000681.2:g.2251978C>T GRCh38
NC_000019.9:g.2251977C>T , CM000681.1:g.2251977C>T GRCh37
NC_000019.8:g.2202977C>T NCBI36
NG_012190.1:g.7865C>T
NG_032853.1:g.9446G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.*21C>T MANE Select ENSP00000221496.2:n.*21C>T
ENST00000221496.4:c.*21C>T ENSP00000221496.2:n.*21C>T
NM_000479.3:c.*21C>T NP_000470.2:n.*21C>T
NM_000479.4:c.*21C>T NP_000470.2:n.*21C>T
NM_000479.5:c.*21C>T MANE Select NP_000470.3:n.*21C>T
Search 100 bp 5'
Search 100 bp 3'