Canonical Allele Identifier: CA447449841
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1008457706
MyVariant Identifiers: chr5:g.156995941C>G (hg19) chr5:g.157568933C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157568933C>G , CM000667.2:g.157568933C>G GRCh38
NC_000005.9:g.156995941C>G , CM000667.1:g.156995941C>G GRCh37
NC_000005.8:g.156928519C>G NCBI36
NG_046960.1:g.11891G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000257527.9:c.180+1962G>C MANE Select ENSP00000257527.5:n.180+1962G>C
ENST00000257527.8:c.180+1962G>C ENSP00000257527.4:n.180+1962G>C
ENST00000517905.1:c.180+1962G>C ENSP00000428654.1:n.180+1962G>C
ENST00000517951.5:c.180+1962G>C ENSP00000428376.1:n.180+1962G>C
NM_033274.4:c.180+1962G>C NP_150377.1:n.180+1962G>C
XM_005266003.2:c.180+1962G>C XP_005266060.1:n.180+1962G>C
NM_033274.5:c.180+1962G>C MANE Select NP_150377.1:n.180+1962G>C
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