Canonical Allele Identifier: CA405301057
Gene: HAMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.35775839A>G (hg19) chr19:g.35284936A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284936A>G , CM000681.2:g.35284936A>G GRCh38
NC_000019.9:g.35775839A>G , CM000681.1:g.35775839A>G GRCh37
NC_000019.8:g.40467679A>G NCBI36
NG_011563.1:g.7430A>G
NG_011563.2:g.7430A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222304.5:c.151-2A>G MANE Select ENSP00000222304.2:n.151-2A>G
ENST00000222304.3:c.151-2A>G ENSP00000222304.2:n.151-2A>G
ENST00000593580.1:n.2420A>G
ENST00000598398.5:c.151-2A>G ENSP00000471894.1:n.151-2A>G
NM_021175.2:c.151-2A>G NP_066998.1:n.151-2A>G
NM_021175.3:c.151-2A>G NP_066998.1:n.151-2A>G
NM_021175.4:c.151-2A>G MANE Select NP_066998.1:n.151-2A>G
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