Canonical Allele Identifier: CA880703362
Gene: AMH HGNC NCBI

Linked Data

dbSNP Id: rs1301257897
MyVariant Identifiers: chr19:g.2251723_2251724insA (hg19) chr19:g.2251724_2251725insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251725dup , CM000681.2:g.2251725dup GRCh38
NC_000019.9:g.2251724dup , CM000681.1:g.2251724dup GRCh37
NC_000019.8:g.2202724dup NCBI36
NG_012190.1:g.7612dup
NG_032853.1:g.9699dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1451dup MANE Select ENSP00000221496.2:p.Ala485GlyfsTer?
ENST00000221496.4:c.1451dup ENSP00000221496.2:p.Ala485GlyfsTer?
NM_000479.3:c.1451dup NP_000470.2:p.Ala485GlyfsTer?
NM_000479.4:c.1451dup NP_000470.2:p.Ala485GlyfsTer?
NM_000479.5:c.1451dup MANE Select NP_000470.3:p.Ala485GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'