Canonical Allele Identifier: CA798286173

Gene: ALB

Linked Data

• dbSNP Id: rs1308691033
• gnomAD v4: 4-73408520-T-C
• MyVariant Identifiers: chr4:g.74274237T>C (hg19) ; chr4:g.73408520T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408520T>C , CM000666.2:g.73408520T>C	GRCh38
NC_000004.11:g.74274237T>C , CM000666.1:g.74274237T>C	GRCh37
NC_000004.10:g.74493101T>C	NCBI36
NG_009291.1:g.9266T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.271-74T>C MANE Select	ENSP00000295897.4:n.271-74T>C
ENST00000295897.8:c.271-74T>C	ENSP00000295897.4:n.271-74T>C
ENST00000401494.7:c.138-835T>C	ENSP00000384695.3:n.138-835T>C
ENST00000415165.6:c.137+3347T>C	ENSP00000401820.2:n.137+3347T>C
ENST00000441319.5:c.277-74T>C	ENSP00000392541.1:n.277-74T>C
ENST00000476441.6:c.80-835T>C	ENSP00000423727.1:n.80-835T>C
ENST00000503124.5:c.33-835T>C	ENSP00000421027.1:n.33-835T>C
ENST00000509063.5:c.271-74T>C	ENSP00000422784.1:n.271-74T>C
ENST00000510166.5:n.307-74T>C
ENST00000514786.1:n.240-74T>C
ENST00000515133.5:n.312-74T>C
ENST00000621085.4:c.271-74T>C	ENSP00000483421.1:n.271-74T>C
ENST00000621628.4:c.271-74T>C	ENSP00000480485.1:n.271-74T>C
NM_000477.5:c.271-74T>C	NP_000468.1:n.271-74T>C
NM_000477.6:c.271-74T>C	NP_000468.1:n.271-74T>C
NM_000477.7:c.271-74T>C MANE Select	NP_000468.1:n.271-74T>C