Canonical Allele Identifier: CA403243125
Gene: AMH HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.2251718C>G (hg19) chr19:g.2251719C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251719C>G , CM000681.2:g.2251719C>G GRCh38
NC_000019.9:g.2251718C>G , CM000681.1:g.2251718C>G GRCh37
NC_000019.8:g.2202718C>G NCBI36
NG_012190.1:g.7606C>G
NG_032853.1:g.9705G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000221496.5:c.1445C>G MANE Select ENSP00000221496.2:p.Thr482Ser
ENST00000221496.4:c.1445C>G ENSP00000221496.2:p.Thr482Ser
NM_000479.3:c.1445C>G NP_000470.2:p.Thr482Ser
NM_000479.4:c.1445C>G NP_000470.2:p.Thr482Ser
NM_000479.5:c.1445C>G MANE Select NP_000470.3:p.Thr482Ser
Search 100 bp 5'
Search 100 bp 3'